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rs387906620

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906620(A;A)
Make rs387906620(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position85487458
GeneNT5E
is asnp
is mentioned by
dbSNPrs387906620
ebirs387906620
HLIrs387906620
Exacrs387906620
Varsomers387906620
Maprs387906620
PheGenIrs387906620
hapmaprs387906620
1000 genomesrs387906620
hgdprs387906620
ensemblrs387906620
gopubmedrs387906620
geneviewrs387906620
scholarrs387906620
googlers387906620
pharmgkbrs387906620
gwascentralrs387906620
openSNPrs387906620
23andMers387906620
23andMe allrs387906620
SNP Nexus

SNPshotrs387906620
SNPdbers387906620
MSV3drs387906620
GWAS Ctlgrs387906620
Max Magnitude0
ClinVar
Risk rs387906620(A;A)
Alt rs387906620(A;A)
Reference rs387906620(G;G)
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.86197176G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000022534.27,