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rs1085307984

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome3
Position122261714
GeneCASR
is asnp
is mentioned by
dbSNPrs1085307984
dbSNP (old)rs1085307984
ClinGenrs1085307984
ebirs1085307984
HLIrs1085307984
Exacrs1085307984
Gnomadrs1085307984
Varsomers1085307984
Maprs1085307984
PheGenIrs1085307984
Biobankrs1085307984
1000 genomesrs1085307984
hgdprs1085307984
ensemblrs1085307984
gopubmedrs1085307984
geneviewrs1085307984
scholarrs1085307984
googlers1085307984
pharmgkbrs1085307984
gwascentralrs1085307984
openSNPrs1085307984
23andMers1085307984
23andMe allrs1085307984
SNPshotrs1085307984
SNPdbers1085307984
MSV3drs1085307984
GWAS Ctlgrs1085307984
Max Magnitude0
ClinVar
Risk rs1085307984(G;G)
Alt rs1085307984(G;G)
Reference Rs1085307984(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CASR
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.121980561C>G
CLNSRC
CLNACC RCV000489801.1,