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rs1057520650

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520650(C;T)
Make rs1057520650(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position32868950
GenePKP2
is asnp
is mentioned by
dbSNPrs1057520650
dbSNP (classic)rs1057520650
ClinGenrs1057520650
ebirs1057520650
HLIrs1057520650
Exacrs1057520650
Gnomadrs1057520650
Varsomers1057520650
LitVarrs1057520650
Maprs1057520650
PheGenIrs1057520650
Biobankrs1057520650
1000 genomesrs1057520650
hgdprs1057520650
ensemblrs1057520650
geneviewrs1057520650
scholarrs1057520650
googlers1057520650
pharmgkbrs1057520650
gwascentralrs1057520650
openSNPrs1057520650
23andMers1057520650
SNPshotrs1057520650
SNPdbers1057520650
MSV3drs1057520650
GWAS Ctlgrs1057520650
Max Magnitude0
ClinVar
Risk rs1057520650(T;T)
Alt rs1057520650(T;T)
Reference Rs1057520650(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PKP2
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.33021884G>A
CLNSRC
CLNACC RCV000418007.1,