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rs747400412

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs747400412(C;T)
Make rs747400412(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position43943793
GeneLRPPRC
is asnp
is mentioned by
dbSNPrs747400412
ebirs747400412
HLIrs747400412
Exacrs747400412
Varsomers747400412
Maprs747400412
PheGenIrs747400412
hapmaprs747400412
1000 genomesrs747400412
hgdprs747400412
ensemblrs747400412
gopubmedrs747400412
geneviewrs747400412
scholarrs747400412
googlers747400412
pharmgkbrs747400412
gwascentralrs747400412
openSNPrs747400412
23andMers747400412
23andMe allrs747400412
SNP Nexus

SNPshotrs747400412
SNPdbers747400412
MSV3drs747400412
GWAS Ctlgrs747400412
Max Magnitude0
ClinVar
Risk rs747400412(T;T)
Alt rs747400412(T;T)
Reference rs747400412(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LRPPRC
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.44170932C>T
CLNSRC
CLNACC RCV000195452.1,