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rs1057520791

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520791(C;C)
Make rs1057520791(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position122284611
GeneCASR
is asnp
is mentioned by
dbSNPrs1057520791
dbSNP (classic)rs1057520791
ClinGenrs1057520791
ebirs1057520791
HLIrs1057520791
Exacrs1057520791
Gnomadrs1057520791
Varsomers1057520791
LitVarrs1057520791
Maprs1057520791
PheGenIrs1057520791
Biobankrs1057520791
1000 genomesrs1057520791
hgdprs1057520791
ensemblrs1057520791
geneviewrs1057520791
scholarrs1057520791
googlers1057520791
pharmgkbrs1057520791
gwascentralrs1057520791
openSNPrs1057520791
23andMers1057520791
23andMe allrs1057520791
SNPshotrs1057520791
SNPdbers1057520791
MSV3drs1057520791
GWAS Ctlgrs1057520791
Max Magnitude0
ClinVar
Risk rs1057520791(C;C)
Alt rs1057520791(C;C)
Reference Rs1057520791(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene CASR
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.122003458G>C
CLNSRC
CLNACC RCV000443461.1,