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rs201934623

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs201934623(C;T)
Make rs201934623(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position67546320
GeneAR
is asnp
is mentioned by
dbSNPrs201934623
ebirs201934623
HLIrs201934623
Exacrs201934623
Varsomers201934623
Maprs201934623
PheGenIrs201934623
hapmaprs201934623
1000 genomesrs201934623
hgdprs201934623
ensemblrs201934623
gopubmedrs201934623
geneviewrs201934623
scholarrs201934623
googlers201934623
pharmgkbrs201934623
gwascentralrs201934623
openSNPrs201934623
23andMers201934623
23andMe allrs201934623
SNP Nexus

SNPshotrs201934623
SNPdbers201934623
MSV3drs201934623
GWAS Ctlgrs201934623
Max Magnitude0
ClinVar
Risk rs201934623(T;T)
Alt rs201934623(T;T)
Reference rs201934623(C;C)
Significance Pathogenic
Disease Reifenstein syndrome
Variation info
Gene AR
CLNDBN Reifenstein syndrome
Reversed 0
HGVS NC_000023.10:g.66766162C>T
CLNSRC
CLNACC RCV000196772.1,