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rs786204422

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786204422(A;A)
Make rs786204422(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position120682101
GeneHGD
is asnp
is mentioned by
dbSNPrs786204422
ebirs786204422
HLIrs786204422
Exacrs786204422
Varsomers786204422
Maprs786204422
PheGenIrs786204422
hapmaprs786204422
1000 genomesrs786204422
hgdprs786204422
ensemblrs786204422
gopubmedrs786204422
geneviewrs786204422
scholarrs786204422
googlers786204422
pharmgkbrs786204422
gwascentralrs786204422
openSNPrs786204422
23andMers786204422
23andMe allrs786204422
SNP Nexus

SNPshotrs786204422
SNPdbers786204422
MSV3drs786204422
GWAS Ctlgrs786204422
Max Magnitude0
ClinVar
Risk rs786204422(A;A)
Alt rs786204422(A;A)
Reference rs786204422(T;T)
Significance Probable-Pathogenic
Disease Alkaptonuria
Variation info
Gene HGD
CLNDBN Alkaptonuria
Reversed 1
HGVS NC_000003.11:g.120400948A>T
CLNSRC
CLNACC RCV000169012.1,