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rs864309635

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs864309635(G;T)
Make rs864309635(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position143923997
GenePLEC
is asnp
is mentioned by
dbSNPrs864309635
ebirs864309635
HLIrs864309635
Exacrs864309635
Varsomers864309635
Maprs864309635
PheGenIrs864309635
hapmaprs864309635
1000 genomesrs864309635
hgdprs864309635
ensemblrs864309635
gopubmedrs864309635
geneviewrs864309635
scholarrs864309635
googlers864309635
pharmgkbrs864309635
gwascentralrs864309635
openSNPrs864309635
23andMers864309635
23andMe allrs864309635
SNP Nexus

SNPshotrs864309635
SNPdbers864309635
MSV3drs864309635
GWAS Ctlgrs864309635
Max Magnitude0
ClinVar
Risk rs864309635(T;T)
Alt rs864309635(T;T)
Reference rs864309635(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PLEC
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.144998165C>A
CLNSRC
CLNACC RCV000203174.1,