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rs1057524792

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057524792(G;G)
Make rs1057524792(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position39467617
GeneLIAS
is asnp
is mentioned by
dbSNPrs1057524792
dbSNP (old)rs1057524792
ClinGenrs1057524792
ebirs1057524792
HLIrs1057524792
Exacrs1057524792
Gnomadrs1057524792
Varsomers1057524792
Maprs1057524792
PheGenIrs1057524792
Biobankrs1057524792
1000 genomesrs1057524792
hgdprs1057524792
ensemblrs1057524792
gopubmedrs1057524792
geneviewrs1057524792
scholarrs1057524792
googlers1057524792
pharmgkbrs1057524792
gwascentralrs1057524792
openSNPrs1057524792
23andMers1057524792
23andMe allrs1057524792
SNPshotrs1057524792
SNPdbers1057524792
MSV3drs1057524792
GWAS Ctlgrs1057524792
Max Magnitude0
ClinVar
Risk rs1057524792(G;G)
Alt rs1057524792(G;G)
Reference Rs1057524792(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LIAS
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.39469237T>G
CLNSRC
CLNACC RCV000426756.1,