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rs1057521112

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057521112(C;C)
Make rs1057521112(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position129528996
GeneRHO
is asnp
is mentioned by
dbSNPrs1057521112
dbSNP (classic)rs1057521112
ClinGenrs1057521112
ebirs1057521112
HLIrs1057521112
Exacrs1057521112
Gnomadrs1057521112
Varsomers1057521112
LitVarrs1057521112
Maprs1057521112
PheGenIrs1057521112
Biobankrs1057521112
1000 genomesrs1057521112
hgdprs1057521112
ensemblrs1057521112
geneviewrs1057521112
scholarrs1057521112
googlers1057521112
pharmgkbrs1057521112
gwascentralrs1057521112
openSNPrs1057521112
23andMers1057521112
23andMe allrs1057521112
SNPshotrs1057521112
SNPdbers1057521112
MSV3drs1057521112
GWAS Ctlgrs1057521112
Max Magnitude0
ClinVar
Risk rs1057521112(C;C)
Alt rs1057521112(C;C)
Reference Rs1057521112(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RHO
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.129247839T>C
CLNSRC
CLNACC RCV000442591.1,