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rs864309634

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs864309634(A;T)
Make rs864309634(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position143916524
GenePLEC
is asnp
is mentioned by
dbSNPrs864309634
ebirs864309634
HLIrs864309634
Exacrs864309634
Varsomers864309634
Maprs864309634
PheGenIrs864309634
hapmaprs864309634
1000 genomesrs864309634
hgdprs864309634
ensemblrs864309634
gopubmedrs864309634
geneviewrs864309634
scholarrs864309634
googlers864309634
pharmgkbrs864309634
gwascentralrs864309634
openSNPrs864309634
23andMers864309634
23andMe allrs864309634
SNP Nexus

SNPshotrs864309634
SNPdbers864309634
MSV3drs864309634
GWAS Ctlgrs864309634
Max Magnitude0
ClinVar
Risk rs864309634(T;T)
Alt rs864309634(T;T)
Reference Rs864309634(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene PLEC
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.144990692T>A
CLNSRC
CLNACC RCV000202942.1,