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rs587776932

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776932(A;A)
Make rs587776932(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position179230077
GenePIK3CA
is asnp
is mentioned by
dbSNPrs587776932
ebirs587776932
HLIrs587776932
Exacrs587776932
Varsomers587776932
Maprs587776932
PheGenIrs587776932
hapmaprs587776932
1000 genomesrs587776932
hgdprs587776932
ensemblrs587776932
gopubmedrs587776932
geneviewrs587776932
scholarrs587776932
googlers587776932
pharmgkbrs587776932
gwascentralrs587776932
openSNPrs587776932
23andMers587776932
23andMe allrs587776932
SNP Nexus

SNPshotrs587776932
SNPdbers587776932
MSV3drs587776932
GWAS Ctlgrs587776932
Max Magnitude0
ClinVar
Risk rs587776932(A;A)
Alt rs587776932(A;A)
Reference rs587776932(G;G)
Significance Other
Disease Megalencephaly cutis marmorata telangiectatica congenita
Variation info
Gene PIK3CA
CLNDBN Megalencephaly cutis marmorata telangiectatica congenita
Reversed 0
HGVS NC_000003.11:g.178947865G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000032907.4,