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rs1057521121

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521121(C;C)
Make rs1057521121(C;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position67643359
GeneAR
is asnp
is mentioned by
dbSNPrs1057521121
dbSNP (classic)rs1057521121
ClinGenrs1057521121
ebirs1057521121
HLIrs1057521121
Exacrs1057521121
Gnomadrs1057521121
Varsomers1057521121
LitVarrs1057521121
Maprs1057521121
PheGenIrs1057521121
Biobankrs1057521121
1000 genomesrs1057521121
hgdprs1057521121
ensemblrs1057521121
geneviewrs1057521121
scholarrs1057521121
googlers1057521121
pharmgkbrs1057521121
gwascentralrs1057521121
openSNPrs1057521121
23andMers1057521121
23andMe allrs1057521121
SNPshotrs1057521121
SNPdbers1057521121
MSV3drs1057521121
GWAS Ctlgrs1057521121
Max Magnitude0
ClinVar
Risk rs1057521121(C;C)
Alt rs1057521121(C;C)
Reference Rs1057521121(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene AR
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.66863201G>C
CLNSRC
CLNACC RCV000431825.1,