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rs1057523748

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057523748(A;T)
Make rs1057523748(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position122283704
GeneCASR
is asnp
is mentioned by
dbSNPrs1057523748
dbSNP (old)rs1057523748
ClinGenrs1057523748
ebirs1057523748
HLIrs1057523748
Exacrs1057523748
Gnomadrs1057523748
Varsomers1057523748
Maprs1057523748
PheGenIrs1057523748
Biobankrs1057523748
1000 genomesrs1057523748
hgdprs1057523748
ensemblrs1057523748
gopubmedrs1057523748
geneviewrs1057523748
scholarrs1057523748
googlers1057523748
pharmgkbrs1057523748
gwascentralrs1057523748
openSNPrs1057523748
23andMers1057523748
23andMe allrs1057523748
SNPshotrs1057523748
SNPdbers1057523748
MSV3drs1057523748
GWAS Ctlgrs1057523748
Max Magnitude0
ClinVar
Risk rs1057523748(T;T)
Alt rs1057523748(T;T)
Reference Rs1057523748(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CASR
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.122002551A>T
CLNSRC
CLNACC RCV000443881.1,