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rs1057523747

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057523747(G;T)
Make rs1057523747(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position67717562
GeneAR
is asnp
is mentioned by
dbSNPrs1057523747
dbSNP (old)rs1057523747
ClinGenrs1057523747
ebirs1057523747
HLIrs1057523747
Exacrs1057523747
Gnomadrs1057523747
Varsomers1057523747
Maprs1057523747
PheGenIrs1057523747
Biobankrs1057523747
1000 genomesrs1057523747
hgdprs1057523747
ensemblrs1057523747
gopubmedrs1057523747
geneviewrs1057523747
scholarrs1057523747
googlers1057523747
pharmgkbrs1057523747
gwascentralrs1057523747
openSNPrs1057523747
23andMers1057523747
23andMe allrs1057523747
SNPshotrs1057523747
SNPdbers1057523747
MSV3drs1057523747
GWAS Ctlgrs1057523747
Max Magnitude0
ClinVar
Risk rs1057523747(T;T)
Alt rs1057523747(T;T)
Reference Rs1057523747(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene AR
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.66937404G>T
CLNSRC
CLNACC RCV000432265.1,