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rs1064793974

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
ChromosomeX
Position48683872
GeneWAS
is asnp
is mentioned by
dbSNPrs1064793974
dbSNP (old)rs1064793974
ClinGenrs1064793974
ebirs1064793974
HLIrs1064793974
Exacrs1064793974
Gnomadrs1064793974
Varsomers1064793974
LitVarrs1064793974
Maprs1064793974
PheGenIrs1064793974
Biobankrs1064793974
1000 genomesrs1064793974
hgdprs1064793974
ensemblrs1064793974
gopubmedrs1064793974
geneviewrs1064793974
scholarrs1064793974
googlers1064793974
pharmgkbrs1064793974
gwascentralrs1064793974
openSNPrs1064793974
23andMers1064793974
23andMe allrs1064793974
SNPshotrs1064793974
SNPdbers1064793974
MSV3drs1064793974
GWAS Ctlgrs1064793974
Max Magnitude0
ClinVar
Risk rs1064793974(T;T)
Alt rs1064793974(T;T)
Reference Rs1064793974(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene WAS
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.48542261G>T
CLNSRC
CLNACC RCV000479329.1,