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rs367891946

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs367891946(C;G)
Make rs367891946(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position40418127
GeneIVD
is asnp
is mentioned by
dbSNPrs367891946
ebirs367891946
HLIrs367891946
Exacrs367891946
Varsomers367891946
Maprs367891946
PheGenIrs367891946
hapmaprs367891946
1000 genomesrs367891946
hgdprs367891946
ensemblrs367891946
gopubmedrs367891946
geneviewrs367891946
scholarrs367891946
googlers367891946
pharmgkbrs367891946
gwascentralrs367891946
openSNPrs367891946
23andMers367891946
23andMe allrs367891946
SNP Nexus

SNPshotrs367891946
SNPdbers367891946
MSV3drs367891946
GWAS Ctlgrs367891946
Max Magnitude0
ClinVar
Risk rs367891946(G;G)
Alt rs367891946(G;G)
Reference rs367891946(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene IVD
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.40710326C>G
CLNSRC
CLNACC RCV000185977.1,