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rs199706677

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199706677(A;A)
Make rs199706677(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position43918330
GeneLRPPRC
is asnp
is mentioned by
dbSNPrs199706677
ebirs199706677
HLIrs199706677
Exacrs199706677
Varsomers199706677
Maprs199706677
PheGenIrs199706677
hapmaprs199706677
1000 genomesrs199706677
hgdprs199706677
ensemblrs199706677
gopubmedrs199706677
geneviewrs199706677
scholarrs199706677
googlers199706677
pharmgkbrs199706677
gwascentralrs199706677
openSNPrs199706677
23andMers199706677
23andMe allrs199706677
SNP Nexus

SNPshotrs199706677
SNPdbers199706677
MSV3drs199706677
GWAS Ctlgrs199706677
Max Magnitude0
ClinVar
Risk rs199706677(A;A)
Alt rs199706677(A;A)
Reference rs199706677(G;G)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene LRPPRC
CLNDBN not specified
Reversed 0
HGVS NC_000002.11:g.44145469G>A
CLNSRC
CLNACC RCV000196348.2,