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rs199727887

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199727887(G;G)
Make rs199727887(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position43977159
GeneLRPPRC
is asnp
is mentioned by
dbSNPrs199727887
ebirs199727887
HLIrs199727887
Exacrs199727887
Varsomers199727887
Maprs199727887
PheGenIrs199727887
hapmaprs199727887
1000 genomesrs199727887
hgdprs199727887
ensemblrs199727887
gopubmedrs199727887
geneviewrs199727887
scholarrs199727887
googlers199727887
pharmgkbrs199727887
gwascentralrs199727887
openSNPrs199727887
23andMers199727887
23andMe allrs199727887
SNP Nexus

SNPshotrs199727887
SNPdbers199727887
MSV3drs199727887
GWAS Ctlgrs199727887
Max Magnitude0
ClinVar
Risk rs199727887(G;G)
Alt rs199727887(G;G)
Reference rs199727887(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LRPPRC
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.44204298T>G
CLNSRC
CLNACC RCV000198242.2,