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rs371525355

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs371525355(C;T)
Make rs371525355(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position153558109
GeneATP2B3
is asnp
is mentioned by
dbSNPrs371525355
ebirs371525355
HLIrs371525355
Exacrs371525355
Varsomers371525355
Maprs371525355
PheGenIrs371525355
hapmaprs371525355
1000 genomesrs371525355
hgdprs371525355
ensemblrs371525355
gopubmedrs371525355
geneviewrs371525355
scholarrs371525355
googlers371525355
pharmgkbrs371525355
gwascentralrs371525355
openSNPrs371525355
23andMers371525355
23andMe allrs371525355
SNP Nexus

SNPshotrs371525355
SNPdbers371525355
MSV3drs371525355
GWAS Ctlgrs371525355
Max Magnitude0
ClinVar
Risk rs371525355(T;T)
Alt rs371525355(T;T)
Reference rs371525355(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ATP2B3
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.152823567C>A
CLNSRC
CLNACC RCV000171447.1,