Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057518247

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057518247(A;G)
Make rs1057518247(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position149212700
GeneCP
is asnp
is mentioned by
dbSNPrs1057518247
dbSNP (old)rs1057518247
ClinGenrs1057518247
ebirs1057518247
HLIrs1057518247
Exacrs1057518247
Gnomadrs1057518247
Varsomers1057518247
Maprs1057518247
PheGenIrs1057518247
Biobankrs1057518247
1000 genomesrs1057518247
hgdprs1057518247
ensemblrs1057518247
gopubmedrs1057518247
geneviewrs1057518247
scholarrs1057518247
googlers1057518247
pharmgkbrs1057518247
gwascentralrs1057518247
openSNPrs1057518247
23andMers1057518247
23andMe allrs1057518247
SNPshotrs1057518247
SNPdbers1057518247
MSV3drs1057518247
GWAS Ctlgrs1057518247
Max Magnitude0
ClinVar
Risk rs1057518247(G;G)
Alt rs1057518247(G;G)
Reference Rs1057518247(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene CP
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.148930487T>C
CLNSRC
CLNACC RCV000414325.1,