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)