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rs786205523

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205523(C;T)
Make rs786205523(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position43948462
GeneLRPPRC
is asnp
is mentioned by
dbSNPrs786205523
ebirs786205523
HLIrs786205523
Exacrs786205523
Varsomers786205523
Maprs786205523
PheGenIrs786205523
hapmaprs786205523
1000 genomesrs786205523
hgdprs786205523
ensemblrs786205523
gopubmedrs786205523
geneviewrs786205523
scholarrs786205523
googlers786205523
pharmgkbrs786205523
gwascentralrs786205523
openSNPrs786205523
23andMers786205523
23andMe allrs786205523
SNP Nexus

SNPshotrs786205523
SNPdbers786205523
MSV3drs786205523
GWAS Ctlgrs786205523
Max Magnitude0
ClinVar
Risk rs786205523(T;T)
Alt rs786205523(T;T)
Reference rs786205523(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LRPPRC
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.44175601G>A
CLNSRC
CLNACC RCV000171290.1,