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rs864309646

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs864309646(C;G)
Make rs864309646(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position135699441
GeneSOHLH1
is asnp
is mentioned by
dbSNPrs864309646
ebirs864309646
HLIrs864309646
Exacrs864309646
Varsomers864309646
Maprs864309646
PheGenIrs864309646
hapmaprs864309646
1000 genomesrs864309646
hgdprs864309646
ensemblrs864309646
gopubmedrs864309646
geneviewrs864309646
scholarrs864309646
googlers864309646
pharmgkbrs864309646
gwascentralrs864309646
openSNPrs864309646
23andMers864309646
23andMe allrs864309646
SNP Nexus

SNPshotrs864309646
SNPdbers864309646
MSV3drs864309646
GWAS Ctlgrs864309646
Max Magnitude0
ClinVar
Risk rs864309646(G;G)
Alt rs864309646(G;G)
Reference rs864309646(C;C)
Significance Probable-Pathogenic
Disease Nonsyndromic hypergonadotropic hypogonadism
Variation info
Gene SOHLH1
CLNDBN Nonsyndromic hypergonadotropic hypogonadism
Reversed 1
HGVS NC_000009.11:g.138591287G>C
CLNSRC Baylor College of Medicine
CLNACC RCV000203231.1,