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rs143370662

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs143370662(A;G)
Make rs143370662(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position120628382
GeneHGD
is asnp
is mentioned by
dbSNPrs143370662
ebirs143370662
HLIrs143370662
Exacrs143370662
Varsomers143370662
Maprs143370662
PheGenIrs143370662
hapmaprs143370662
1000 genomesrs143370662
hgdprs143370662
ensemblrs143370662
gopubmedrs143370662
geneviewrs143370662
scholarrs143370662
googlers143370662
pharmgkbrs143370662
gwascentralrs143370662
openSNPrs143370662
23andMers143370662
23andMe allrs143370662
SNP Nexus

SNPshotrs143370662
SNPdbers143370662
MSV3drs143370662
GWAS Ctlgrs143370662
Max Magnitude0
ClinVar
Risk rs143370662(G;G)
Alt rs143370662(G;G)
Reference rs143370662(A;A)
Significance Probable-Pathogenic
Disease Alkaptonuria
Variation info
Gene HGD
CLNDBN Alkaptonuria
Reversed 0
HGVS NC_000003.11:g.120347229A>G
CLNSRC
CLNACC RCV000169039.1,