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rs797044903

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GGGCCAA;GGGCCAA) 0 common in clinvar
Make rs797044903(-;-)
Make rs797044903(-;GGGCCAA)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position38132883
GenePLA2G6
is asnp
is mentioned by
dbSNPrs797044903
ClinGenrs797044903
ebirs797044903
HLIrs797044903
Exacrs797044903
Varsomers797044903
Maprs797044903
PheGenIrs797044903
hapmaprs797044903
1000 genomesrs797044903
hgdprs797044903
ensemblrs797044903
gopubmedrs797044903
geneviewrs797044903
scholarrs797044903
googlers797044903
pharmgkbrs797044903
gwascentralrs797044903
openSNPrs797044903
23andMers797044903
23andMe allrs797044903
SNP Nexus

SNPshotrs797044903
SNPdbers797044903
MSV3drs797044903
GWAS Ctlgrs797044903
Max Magnitude0
ClinVar
Risk rs797044903(-;-)
Alt rs797044903(-;-)
Reference Rs797044903(GGGCCAA;GGGCCAA)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene PLA2G6
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000022.10:g.38528890_38528896delTTGGCCC
CLNSRC
CLNACC RCV000190729.1,