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rs373328681

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs373328681(A;A)
Make rs373328681(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position85471336
GeneNT5E
is asnp
is mentioned by
dbSNPrs373328681
ebirs373328681
HLIrs373328681
Exacrs373328681
Varsomers373328681
Maprs373328681
PheGenIrs373328681
hapmaprs373328681
1000 genomesrs373328681
hgdprs373328681
ensemblrs373328681
gopubmedrs373328681
geneviewrs373328681
scholarrs373328681
googlers373328681
pharmgkbrs373328681
gwascentralrs373328681
openSNPrs373328681
23andMers373328681
23andMe allrs373328681
SNP Nexus

SNPshotrs373328681
SNPdbers373328681
MSV3drs373328681
GWAS Ctlgrs373328681
Max Magnitude0
ClinVar
Risk rs373328681(A,T;A,T)
Alt rs373328681(A,T;A,T)
Reference rs373328681(C;C)
Significance Pathogenic
Disease Calcification of joints and arteries
Variation info
Gene NT5E
CLNDBN Calcification of joints and arteries
Reversed 0
HGVS NC_000006.11:g.86181054C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000022533.27,