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rs1057518102

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518102(A;A)
Make rs1057518102(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position49862043
GenePNKP
is asnp
is mentioned by
dbSNPrs1057518102
dbSNP (old)rs1057518102
ClinGenrs1057518102
ebirs1057518102
HLIrs1057518102
Exacrs1057518102
Gnomadrs1057518102
Varsomers1057518102
LitVarrs1057518102
Maprs1057518102
PheGenIrs1057518102
Biobankrs1057518102
1000 genomesrs1057518102
hgdprs1057518102
ensemblrs1057518102
gopubmedrs1057518102
geneviewrs1057518102
scholarrs1057518102
googlers1057518102
pharmgkbrs1057518102
gwascentralrs1057518102
openSNPrs1057518102
23andMers1057518102
23andMe allrs1057518102
SNPshotrs1057518102
SNPdbers1057518102
MSV3drs1057518102
GWAS Ctlgrs1057518102
Max Magnitude0
ClinVar
Risk rs1057518102(A;A)
Alt rs1057518102(A;A)
Reference Rs1057518102(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PNKP
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.50365300C>T
CLNSRC
CLNACC RCV000413872.1,