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rs727503964

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs727503964(G;G)
Make rs727503964(G;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position134498438
GeneHPRT1
is asnp
is mentioned by
dbSNPrs727503964
ebirs727503964
HLIrs727503964
Exacrs727503964
Varsomers727503964
Maprs727503964
PheGenIrs727503964
hapmaprs727503964
1000 genomesrs727503964
hgdprs727503964
ensemblrs727503964
gopubmedrs727503964
geneviewrs727503964
scholarrs727503964
googlers727503964
pharmgkbrs727503964
gwascentralrs727503964
openSNPrs727503964
23andMers727503964
23andMe allrs727503964
SNP Nexus

SNPshotrs727503964
SNPdbers727503964
MSV3drs727503964
GWAS Ctlgrs727503964
Max Magnitude0
ClinVar
Risk rs727503964(G;G)
Alt rs727503964(G;G)
Reference rs727503964(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene HPRT1
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.133632468T>G
CLNSRC
CLNACC RCV000153368.3,