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rs547175863

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs547175863(C;C)
Make rs547175863(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome22
Position38115582
GenePLA2G6
is asnp
is mentioned by
dbSNPrs547175863
dbSNP (classic)rs547175863
ClinGenrs547175863
ebirs547175863
HLIrs547175863
Exacrs547175863
Gnomadrs547175863
Varsomers547175863
LitVarrs547175863
Maprs547175863
PheGenIrs547175863
Biobankrs547175863
1000 genomesrs547175863
hgdprs547175863
ensemblrs547175863
geneviewrs547175863
scholarrs547175863
googlers547175863
pharmgkbrs547175863
gwascentralrs547175863
openSNPrs547175863
23andMers547175863
SNPshotrs547175863
SNPdbers547175863
MSV3drs547175863
GWAS Ctlgrs547175863
Max Magnitude0
ClinVar
Risk rs547175863(C;C)
Alt rs547175863(C;C)
Reference Rs547175863(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PLA2G6
CLNDBN not provided
Reversed 0
HGVS NC_000022.10:g.38511589G>C
CLNSRC
CLNACC RCV000412988.1,