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rs1057518061

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518061(C;C)
Make rs1057518061(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome18
Position62138238
GenePIGN
is asnp
is mentioned by
dbSNPrs1057518061
dbSNP (old)rs1057518061
ClinGenrs1057518061
ebirs1057518061
HLIrs1057518061
Exacrs1057518061
Gnomadrs1057518061
Varsomers1057518061
Maprs1057518061
PheGenIrs1057518061
Biobankrs1057518061
1000 genomesrs1057518061
hgdprs1057518061
ensemblrs1057518061
gopubmedrs1057518061
geneviewrs1057518061
scholarrs1057518061
googlers1057518061
pharmgkbrs1057518061
gwascentralrs1057518061
openSNPrs1057518061
23andMers1057518061
23andMe allrs1057518061
SNPshotrs1057518061
SNPdbers1057518061
MSV3drs1057518061
GWAS Ctlgrs1057518061
Max Magnitude0
ClinVar
Risk rs1057518061(C;C)
Alt rs1057518061(C;C)
Reference Rs1057518061(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PIGN
CLNDBN not provided
Reversed 1
HGVS NC_000018.9:g.59805471C>G
CLNSRC
CLNACC RCV000413707.1,