SNP Report

Basic Info
| Name |
rs72774047
dbSNP
Ensembl
|
| Location |
16:9998941 - 9998941(+) |
| Variant Seq |
A |
| Ancestral Allele |
G |
| Ref Seq |
G |
| Minor Allele Frequence |
0.0403355 |
| Annotation |
intron_variant; non_coding_transcript_variant
|
| Variant Effect |
intron_variant(ENST00000396573, ENST00000562109, ENST00000566670, ENST00000566683, ENST00000330684, ENST00000568247); non_coding_transcript_variant(ENST00000566670, ENST00000566683, ENST00000568247)
|
| SIFT Annotation |
tolerated
|
| SIFT Variant Effect |
tolerated(ENST00000396573, ENST00000330684, ENST00000396575, ENST00000562109, ENST00000535259)
|
| PolyPhen Annotation |
benign; probably_damaging
|
| PolyPhen Variant Effect |
benign(ENST00000396573, ENST00000330684, ENST00000562109, ENST00000535259); probably_damaging(ENST00000396575)
|
| rSNP? |
Yes
Link in rVarBase
|
| Related Regulatory Elements |
n/a
|
| Chromatin State |
Weak transcription
|
| 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 rs72774047 (count: 0)

SNP related eQTL (count: 1)