SNP Report

Basic Info
| Name |
rs3810595
dbSNP
Ensembl
|
| Location |
22:19962121 - 19962121(+) |
| Variant Seq |
C |
| Ancestral Allele |
C |
| Ref Seq |
G |
| Minor Allele Frequence |
0.356629 |
| Annotation |
upstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant
|
| Variant Effect |
upstream_gene_variant(ENST00000428707, ENST00000493893, ENST00000585066, ENST00000449653); intron_variant(ENST00000406520, ENST00000207636, ENST00000403710, ENST00000403184, ENST00000361682, ENST00000407537, ENST00000467943, ENST00000412786); NMD_transcript_variant(ENST00000207636); non_coding_transcript_variant(ENST00000467943)
|
| SIFT Annotation |
tolerated
|
| SIFT Variant Effect |
tolerated(ENST00000406520, ENST00000412786, ENST00000361682, ENST00000207636, ENST00000407537, ENST00000449653, ENST00000403184, ENST00000403710)
|
| PolyPhen Annotation |
benign
|
| PolyPhen Variant Effect |
benign(ENST00000406520, ENST00000412786, ENST00000361682, ENST00000207636, ENST00000407537, ENST00000449653, ENST00000403184, ENST00000403710)
|
| rSNP? |
No
Link in rVarBase
|
| Related Regulatory Elements |
N.A.
|
| Chromatin State |
N.A.
|
| No. of Marker's Association Results |
0 (Positive: 0; Negative: 0; Trend: 0) |
| Source |
LD-proxy |

SNP related association results

SNP related genes (count: 1)

SNPs in LD with rs3810595 (count: 0)

SNP related eQTL (count: 1)