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rs750324117

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs750324117(G;T)
Make rs750324117(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position67546011
GeneAR
is asnp
is mentioned by
dbSNPrs750324117
dbSNP (classic)rs750324117
ClinGenrs750324117
ebirs750324117
HLIrs750324117
Exacrs750324117
Gnomadrs750324117
Varsomers750324117
LitVarrs750324117
Maprs750324117
PheGenIrs750324117
Biobankrs750324117
1000 genomesrs750324117
hgdprs750324117
ensemblrs750324117
geneviewrs750324117
scholarrs750324117
googlers750324117
pharmgkbrs750324117
gwascentralrs750324117
openSNPrs750324117
23andMers750324117
SNPshotrs750324117
SNPdbers750324117
MSV3drs750324117
GWAS Ctlgrs750324117
Max Magnitude0
ClinVar
Risk rs750324117(A;A) rs750324117(T;T)
Alt rs750324117(A;A) rs750324117(T;T)
Reference Rs750324117(G;G)
Significance Pathogenic
Disease Androgen resistance syndrome
Variation info
Gene AR
CLNDBN Androgen resistance syndrome
Reversed 0
HGVS NC_000023.10:g.66765853G>T
CLNSRC
CLNACC RCV000415036.1,