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rs190007694

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs190007694(G;G)
Make rs190007694(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position43946109
GeneLRPPRC
is asnp
is mentioned by
dbSNPrs190007694
ebirs190007694
HLIrs190007694
Exacrs190007694
Varsomers190007694
Maprs190007694
PheGenIrs190007694
hapmaprs190007694
1000 genomesrs190007694
hgdprs190007694
ensemblrs190007694
gopubmedrs190007694
geneviewrs190007694
scholarrs190007694
googlers190007694
pharmgkbrs190007694
gwascentralrs190007694
openSNPrs190007694
23andMers190007694
23andMe allrs190007694
SNP Nexus

SNPshotrs190007694
SNPdbers190007694
MSV3drs190007694
GWAS Ctlgrs190007694
Max Magnitude0
ClinVar
Risk rs190007694(G;G)
Alt rs190007694(G;G)
Reference rs190007694(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LRPPRC
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.44173248T>G
CLNSRC
CLNACC RCV000199688.1,