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rs765911841

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs765911841(C;C)
Make rs765911841(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position43976185
GeneLRPPRC
is asnp
is mentioned by
dbSNPrs765911841
ebirs765911841
HLIrs765911841
Exacrs765911841
Varsomers765911841
Maprs765911841
PheGenIrs765911841
hapmaprs765911841
1000 genomesrs765911841
hgdprs765911841
ensemblrs765911841
gopubmedrs765911841
geneviewrs765911841
scholarrs765911841
googlers765911841
pharmgkbrs765911841
gwascentralrs765911841
openSNPrs765911841
23andMers765911841
23andMe allrs765911841
SNP Nexus

SNPshotrs765911841
SNPdbers765911841
MSV3drs765911841
GWAS Ctlgrs765911841
Max Magnitude0
ClinVar
Risk rs765911841(C;C)
Alt rs765911841(C;C)
Reference rs765911841(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LRPPRC
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.44203324T>C
CLNSRC
CLNACC RCV000200430.1,