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rs878853033

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs878853033(G;G)
Make rs878853033(G;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position67686045
GeneAR
is asnp
is mentioned by
dbSNPrs878853033
ebirs878853033
HLIrs878853033
Exacrs878853033
Varsomers878853033
Maprs878853033
PheGenIrs878853033
hapmaprs878853033
1000 genomesrs878853033
hgdprs878853033
ensemblrs878853033
gopubmedrs878853033
geneviewrs878853033
scholarrs878853033
googlers878853033
pharmgkbrs878853033
gwascentralrs878853033
openSNPrs878853033
23andMers878853033
23andMe allrs878853033
SNP Nexus

SNPshotrs878853033
SNPdbers878853033
MSV3drs878853033
GWAS Ctlgrs878853033
Max Magnitude0
ClinVar
Risk rs878853033(G;G)
Alt rs878853033(G;G)
Reference rs878853033(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene AR
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.66905887T>G
CLNSRC
CLNACC RCV000224290.1,