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rs137853226

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137853226(C;T)
Make rs137853226(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position50256262
GeneGNAI2
is asnp
is mentioned by
dbSNPrs137853226
ebirs137853226
HLIrs137853226
Exacrs137853226
Varsomers137853226
Maprs137853226
PheGenIrs137853226
hapmaprs137853226
1000 genomesrs137853226
hgdprs137853226
ensemblrs137853226
gopubmedrs137853226
geneviewrs137853226
scholarrs137853226
googlers137853226
pharmgkbrs137853226
gwascentralrs137853226
openSNPrs137853226
23andMers137853226
23andMe allrs137853226
SNP Nexus

SNPshotrs137853226
SNPdbers137853226
MSV3drs137853226
GWAS Ctlgrs137853226
Merged fromRs28933075
Max Magnitude0
OMIM139360
Desc
Variant0001
Relatedalso
OMIM139360
Desc
Variant0003
Relatedalso
ClinVar
Risk rs137853226(G,T;G,T)
Alt rs137853226(G,T;G,T)
Reference rs137853226(C;C)
Significance Pathogenic
Disease Pituitary dependent hypercortisolism Adrenocortical tumor Granulosa cell tumor of the ovary Thecoma
Variation info
Gene GNAI2
CLNDBN Pituitary dependent hypercortisolism Adrenocortical tumor, somatic Granulosa cell tumor of the ovary Thecoma, somatic
Reversed 0
HGVS NC_000003.11:g.50293694C>G; NC_000003.11:g.50293694C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017256.4, RCV000017250.4, RCV000017251.4, RCV000017252.4,