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rs1057521129

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057521129(A;G)
Make rs1057521129(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position122284385
GeneCASR
is asnp
is mentioned by
dbSNPrs1057521129
dbSNP (old)rs1057521129
ClinGenrs1057521129
ebirs1057521129
HLIrs1057521129
Exacrs1057521129
Gnomadrs1057521129
Varsomers1057521129
Maprs1057521129
PheGenIrs1057521129
Biobankrs1057521129
1000 genomesrs1057521129
hgdprs1057521129
ensemblrs1057521129
gopubmedrs1057521129
geneviewrs1057521129
scholarrs1057521129
googlers1057521129
pharmgkbrs1057521129
gwascentralrs1057521129
openSNPrs1057521129
23andMers1057521129
23andMe allrs1057521129
SNPshotrs1057521129
SNPdbers1057521129
MSV3drs1057521129
GWAS Ctlgrs1057521129
Max Magnitude0
ClinVar
Risk rs1057521129(G;G)
Alt rs1057521129(G;G)
Reference Rs1057521129(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CASR
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.122003232A>G
CLNSRC
CLNACC RCV000440135.1,