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rs1057517712

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057517712(C;C)
Make rs1057517712(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position122262218
GeneCASR
is asnp
is mentioned by
dbSNPrs1057517712
dbSNP (old)rs1057517712
ClinGenrs1057517712
ebirs1057517712
HLIrs1057517712
Exacrs1057517712
Gnomadrs1057517712
Varsomers1057517712
Maprs1057517712
PheGenIrs1057517712
Biobankrs1057517712
1000 genomesrs1057517712
hgdprs1057517712
ensemblrs1057517712
gopubmedrs1057517712
geneviewrs1057517712
scholarrs1057517712
googlers1057517712
pharmgkbrs1057517712
gwascentralrs1057517712
openSNPrs1057517712
23andMers1057517712
23andMe allrs1057517712
SNPshotrs1057517712
SNPdbers1057517712
MSV3drs1057517712
GWAS Ctlgrs1057517712
Max Magnitude0
ClinVar
Risk rs1057517712(C;C)
Alt rs1057517712(C;C)
Reference Rs1057517712(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CASR
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.121981065T>C
CLNSRC
CLNACC RCV000413522.1,