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rs587776800

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CA;CA) 0 common in clinvar
Make rs587776800(-;-)
Make rs587776800(-;CA)
ReferenceGRCh38 38.1/142
Chromosome1
Position19978420
GenePLA2G2A
is asnp
is mentioned by
dbSNPrs587776800
ebirs587776800
HLIrs587776800
Exacrs587776800
Varsomers587776800
Maprs587776800
PheGenIrs587776800
hapmaprs587776800
1000 genomesrs587776800
hgdprs587776800
ensemblrs587776800
gopubmedrs587776800
geneviewrs587776800
scholarrs587776800
googlers587776800
pharmgkbrs587776800
gwascentralrs587776800
openSNPrs587776800
23andMers587776800
23andMe allrs587776800
SNP Nexus

SNPshotrs587776800
SNPdbers587776800
MSV3drs587776800
GWAS Ctlgrs587776800
Max Magnitude0
ClinVar
Risk rs587776800(;)
Alt rs587776800(;)
Reference rs587776800(CA;CA)
Significance Pathogenic
Disease Familial colorectal cancer
Variation info
Gene PLA2G2A
CLNDBN Familial colorectal cancer
Reversed 0
HGVS NC_000001.10:g.20304913_20304914delCA
CLNSRC OMIM Allelic Variant
CLNACC RCV000014605.24,