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rs186924074

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs186924074(A;G)
Make rs186924074(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position51961861
GeneATP7B
is asnp
is mentioned by
dbSNPrs186924074
dbSNP (classic)rs186924074
ClinGenrs186924074
ebirs186924074
HLIrs186924074
Exacrs186924074
Gnomadrs186924074
Varsomers186924074
LitVarrs186924074
Maprs186924074
PheGenIrs186924074
Biobankrs186924074
1000 genomesrs186924074
hgdprs186924074
ensemblrs186924074
geneviewrs186924074
scholarrs186924074
googlers186924074
pharmgkbrs186924074
gwascentralrs186924074
openSNPrs186924074
23andMers186924074
23andMe allrs186924074
SNPshotrs186924074
SNPdbers186924074
MSV3drs186924074
GWAS Ctlgrs186924074
Max Magnitude0
ClinVar
Risk rs186924074(G;G)
Alt rs186924074(G;G)
Reference Rs186924074(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ATP7B
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.52535997A>G
CLNSRC
CLNACC RCV000480322.1,