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rs200686732

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs200686732(C;T)
Make rs200686732(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position43995941
GeneLRPPRC
is asnp
is mentioned by
dbSNPrs200686732
ebirs200686732
HLIrs200686732
Exacrs200686732
Varsomers200686732
Maprs200686732
PheGenIrs200686732
hapmaprs200686732
1000 genomesrs200686732
hgdprs200686732
ensemblrs200686732
gopubmedrs200686732
geneviewrs200686732
scholarrs200686732
googlers200686732
pharmgkbrs200686732
gwascentralrs200686732
openSNPrs200686732
23andMers200686732
23andMe allrs200686732
SNP Nexus

SNPshotrs200686732
SNPdbers200686732
MSV3drs200686732
GWAS Ctlgrs200686732
Max Magnitude0
ClinVar
Risk rs200686732(A,G,T;A,G,T)
Alt rs200686732(A,G,T;A,G,T)
Reference rs200686732(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LRPPRC
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.44223080C>T
CLNSRC
CLNACC RCV000199897.1,