Have questions? Visit https://www.reddit.com/r/SNPedia

rs137853227

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853227(A;A)
Make rs137853227(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position50256263
GeneGNAI2
is asnp
is mentioned by
dbSNPrs137853227
ebirs137853227
HLIrs137853227
Exacrs137853227
Varsomers137853227
Maprs137853227
PheGenIrs137853227
hapmaprs137853227
1000 genomesrs137853227
hgdprs137853227
ensemblrs137853227
gopubmedrs137853227
geneviewrs137853227
scholarrs137853227
googlers137853227
pharmgkbrs137853227
gwascentralrs137853227
openSNPrs137853227
23andMers137853227
23andMe allrs137853227
SNP Nexus

SNPshotrs137853227
SNPdbers137853227
MSV3drs137853227
GWAS Ctlgrs137853227
Max Magnitude0
OMIM139360
Desc
Variant0002
Relatedalso
ClinVar
Risk rs137853227(A;A)
Alt rs137853227(A;A)
Reference rs137853227(G;G)
Significance Pathogenic
Disease Adrenocortical tumor Granulosa cell tumor of the ovary Thecoma
Variation info
Gene GNAI2
CLNDBN Adrenocortical tumor, somatic Granulosa cell tumor of the ovary Thecoma, somatic
Reversed 0
HGVS NC_000003.11:g.50293695G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017253.3, RCV000017254.3, RCV000017255.3,