SNP Report

Basic Info
Name |
rs61938733
dbSNP
Ensembl
|
Location |
12:117349366 - 117349366(+) |
Variant Seq |
A |
Ancestral Allele |
G |
Ref Seq |
G |
Minor Allele Frequence |
0.0155751 |
Annotation |
intron_variant; non_coding_transcript_variant
|
Variant Effect |
intron_variant(ENST00000618760, ENST00000549189, ENST00000317775, ENST00000477584); non_coding_transcript_variant(ENST00000549189, ENST00000477584)
|
SIFT Annotation |
deleterious_-_low_confidence
|
SIFT Variant Effect |
deleterious_-_low_confidence(ENST00000317775, ENST00000338101, ENST00000618760, ENST00000344089)
|
PolyPhen Annotation |
probably_damaging
|
PolyPhen Variant Effect |
probably_damaging(ENST00000317775, ENST00000338101, ENST00000618760, ENST00000344089)
|
rSNP? |
Yes
Link in rVarBase
|
Related Regulatory Elements |
n/a
|
Chromatin State |
Weak transcription;Enhancers
|
No. of Marker's Association Results |
1 (Positive: 0; Negative: 1; Trend: 0) |
Source |
Literature |

SNP related association results

SNP related genes (count: 1)

SNPs in LD with rs61938733 (count: 0)

SNP related eQTL (count: 1)