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rs1057521122

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057521122(A;G)
Make rs1057521122(G;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position67722881
GeneAR
is asnp
is mentioned by
dbSNPrs1057521122
dbSNP (old)rs1057521122
ClinGenrs1057521122
ebirs1057521122
HLIrs1057521122
Exacrs1057521122
Gnomadrs1057521122
Varsomers1057521122
Maprs1057521122
PheGenIrs1057521122
Biobankrs1057521122
1000 genomesrs1057521122
hgdprs1057521122
ensemblrs1057521122
gopubmedrs1057521122
geneviewrs1057521122
scholarrs1057521122
googlers1057521122
pharmgkbrs1057521122
gwascentralrs1057521122
openSNPrs1057521122
23andMers1057521122
23andMe allrs1057521122
SNPshotrs1057521122
SNPdbers1057521122
MSV3drs1057521122
GWAS Ctlgrs1057521122
Max Magnitude0
ClinVar
Risk rs1057521122(G;G)
Alt rs1057521122(G;G)
Reference Rs1057521122(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene AR
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.66942723A>G
CLNSRC
CLNACC RCV000441243.1,