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rs1057517811

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057517811(A;G)
Make rs1057517811(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position112233200
GenePTS
is asnp
is mentioned by
dbSNPrs1057517811
dbSNP (old)rs1057517811
ClinGenrs1057517811
ebirs1057517811
HLIrs1057517811
Exacrs1057517811
Gnomadrs1057517811
Varsomers1057517811
Maprs1057517811
PheGenIrs1057517811
Biobankrs1057517811
1000 genomesrs1057517811
hgdprs1057517811
ensemblrs1057517811
gopubmedrs1057517811
geneviewrs1057517811
scholarrs1057517811
googlers1057517811
pharmgkbrs1057517811
gwascentralrs1057517811
openSNPrs1057517811
23andMers1057517811
23andMe allrs1057517811
SNPshotrs1057517811
SNPdbers1057517811
MSV3drs1057517811
GWAS Ctlgrs1057517811
Max Magnitude0
ClinVar
Risk rs1057517811(G;G)
Alt rs1057517811(G;G)
Reference Rs1057517811(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PTS
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.112103923A>G
CLNSRC
CLNACC RCV000413988.1,