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rs1057524862

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057524862(A;A)
Make rs1057524862(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position66863875
GenePC
is asnp
is mentioned by
dbSNPrs1057524862
dbSNP (old)rs1057524862
ClinGenrs1057524862
ebirs1057524862
HLIrs1057524862
Exacrs1057524862
Gnomadrs1057524862
Varsomers1057524862
LitVarrs1057524862
Maprs1057524862
PheGenIrs1057524862
Biobankrs1057524862
1000 genomesrs1057524862
hgdprs1057524862
ensemblrs1057524862
gopubmedrs1057524862
geneviewrs1057524862
scholarrs1057524862
googlers1057524862
pharmgkbrs1057524862
gwascentralrs1057524862
openSNPrs1057524862
23andMers1057524862
23andMe allrs1057524862
SNPshotrs1057524862
SNPdbers1057524862
MSV3drs1057524862
GWAS Ctlgrs1057524862
Max Magnitude0
ClinVar
Risk rs1057524862(A;A)
Alt rs1057524862(A;A)
Reference Rs1057524862(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PC
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.66631346C>T
CLNSRC
CLNACC RCV000429009.1,