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rs774221179

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs774221179(A;A)
Make rs774221179(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position51974889
GeneATP7B
is asnp
is mentioned by
dbSNPrs774221179
ebirs774221179
HLIrs774221179
Exacrs774221179
Varsomers774221179
Maprs774221179
PheGenIrs774221179
hapmaprs774221179
1000 genomesrs774221179
hgdprs774221179
ensemblrs774221179
gopubmedrs774221179
geneviewrs774221179
scholarrs774221179
googlers774221179
pharmgkbrs774221179
gwascentralrs774221179
openSNPrs774221179
23andMers774221179
23andMe allrs774221179
SNP Nexus

SNPshotrs774221179
SNPdbers774221179
MSV3drs774221179
GWAS Ctlgrs774221179
Max Magnitude0
ClinVar
Risk rs774221179(A;A)
Alt rs774221179(A;A)
Reference rs774221179(G;G)
Significance Probable-Pathogenic
Disease Wilson's disease
Variation info
Gene ATP7B
CLNDBN Wilson's disease
Reversed 0
HGVS NC_000013.10:g.52549025G>A
CLNSRC
CLNACC RCV000169259.1,