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rs1057520557

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520557(G;T)
Make rs1057520557(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position122283782
GeneCASR
is asnp
is mentioned by
dbSNPrs1057520557
dbSNP (classic)rs1057520557
ClinGenrs1057520557
ebirs1057520557
HLIrs1057520557
Exacrs1057520557
Gnomadrs1057520557
Varsomers1057520557
LitVarrs1057520557
Maprs1057520557
PheGenIrs1057520557
Biobankrs1057520557
1000 genomesrs1057520557
hgdprs1057520557
ensemblrs1057520557
geneviewrs1057520557
scholarrs1057520557
googlers1057520557
pharmgkbrs1057520557
gwascentralrs1057520557
openSNPrs1057520557
23andMers1057520557
23andMe allrs1057520557
SNPshotrs1057520557
SNPdbers1057520557
MSV3drs1057520557
GWAS Ctlgrs1057520557
Max Magnitude0
ClinVar
Risk rs1057520557(T;T)
Alt rs1057520557(T;T)
Reference Rs1057520557(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene CASR
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.122002629G>T
CLNSRC
CLNACC RCV000429289.1,