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rs1057520646

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520646(G;T)
Make rs1057520646(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position122284565
GeneCASR
is asnp
is mentioned by
dbSNPrs1057520646
dbSNP (old)rs1057520646
ClinGenrs1057520646
ebirs1057520646
HLIrs1057520646
Exacrs1057520646
Gnomadrs1057520646
Varsomers1057520646
LitVarrs1057520646
Maprs1057520646
PheGenIrs1057520646
Biobankrs1057520646
1000 genomesrs1057520646
hgdprs1057520646
ensemblrs1057520646
gopubmedrs1057520646
geneviewrs1057520646
scholarrs1057520646
googlers1057520646
pharmgkbrs1057520646
gwascentralrs1057520646
openSNPrs1057520646
23andMers1057520646
23andMe allrs1057520646
SNPshotrs1057520646
SNPdbers1057520646
MSV3drs1057520646
GWAS Ctlgrs1057520646
Max Magnitude0
ClinVar
Risk rs1057520646(T;T)
Alt rs1057520646(T;T)
Reference Rs1057520646(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene CASR
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.122003412G>T
CLNSRC
CLNACC RCV000441373.1,