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rs1057520235

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057520235(C;C)
Make rs1057520235(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position51950277
GeneATP7B
is asnp
is mentioned by
dbSNPrs1057520235
dbSNP (old)rs1057520235
ClinGenrs1057520235
ebirs1057520235
HLIrs1057520235
Exacrs1057520235
Gnomadrs1057520235
Varsomers1057520235
Maprs1057520235
PheGenIrs1057520235
Biobankrs1057520235
1000 genomesrs1057520235
hgdprs1057520235
ensemblrs1057520235
gopubmedrs1057520235
geneviewrs1057520235
scholarrs1057520235
googlers1057520235
pharmgkbrs1057520235
gwascentralrs1057520235
openSNPrs1057520235
23andMers1057520235
23andMe allrs1057520235
SNPshotrs1057520235
SNPdbers1057520235
MSV3drs1057520235
GWAS Ctlgrs1057520235
Max Magnitude0
ClinVar
Risk rs1057520235(C;C)
Alt rs1057520235(C;C)
Reference Rs1057520235(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ATP7B
CLNDBN not provided
Reversed 1
HGVS NC_000013.10:g.52524413A>G
CLNSRC
CLNACC RCV000430661.1,