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rs368215361

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs368215361(C;G)
Make rs368215361(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position153565099
GeneATP2B3
is asnp
is mentioned by
dbSNPrs368215361
ebirs368215361
HLIrs368215361
Exacrs368215361
Varsomers368215361
Maprs368215361
PheGenIrs368215361
hapmaprs368215361
1000 genomesrs368215361
hgdprs368215361
ensemblrs368215361
gopubmedrs368215361
geneviewrs368215361
scholarrs368215361
googlers368215361
pharmgkbrs368215361
gwascentralrs368215361
openSNPrs368215361
23andMers368215361
23andMe allrs368215361
SNP Nexus

SNPshotrs368215361
SNPdbers368215361
MSV3drs368215361
GWAS Ctlgrs368215361
Max Magnitude0
ClinVar
Risk rs368215361(G;G)
Alt rs368215361(G;G)
Reference rs368215361(C;C)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene ATP2B3
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000023.10:g.152830557C>T
CLNSRC
CLNACC RCV000210622.1,