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rs376324882

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs376324882(A;A)
Make rs376324882(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position40410756
GeneIVD
is asnp
is mentioned by
dbSNPrs376324882
ebirs376324882
HLIrs376324882
Exacrs376324882
Varsomers376324882
Maprs376324882
PheGenIrs376324882
hapmaprs376324882
1000 genomesrs376324882
hgdprs376324882
ensemblrs376324882
gopubmedrs376324882
geneviewrs376324882
scholarrs376324882
googlers376324882
pharmgkbrs376324882
gwascentralrs376324882
openSNPrs376324882
23andMers376324882
23andMe allrs376324882
SNP Nexus

SNPshotrs376324882
SNPdbers376324882
MSV3drs376324882
GWAS Ctlgrs376324882
Max Magnitude0
ClinVar
Risk rs376324882(A,T;A,T)
Alt rs376324882(A,T;A,T)
Reference rs376324882(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene IVD
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.40702955C>T
CLNSRC
CLNACC RCV000185983.1,