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rs587777184

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777184(A;A)
Make rs587777184(A;G)
ReferenceGRCh38 38.1/142
Chromosome19
Position7540675
GenePNPLA6
is asnp
is mentioned by
dbSNPrs587777184
ebirs587777184
HLIrs587777184
Exacrs587777184
Varsomers587777184
Maprs587777184
PheGenIrs587777184
hapmaprs587777184
1000 genomesrs587777184
hgdprs587777184
ensemblrs587777184
gopubmedrs587777184
geneviewrs587777184
scholarrs587777184
googlers587777184
pharmgkbrs587777184
gwascentralrs587777184
openSNPrs587777184
23andMers587777184
23andMe allrs587777184
SNP Nexus

SNPshotrs587777184
SNPdbers587777184
MSV3drs587777184
GWAS Ctlgrs587777184
Max Magnitude0
ClinVar
Risk rs587777184(A;A)
Alt rs587777184(A;A)
Reference rs587777184(G;G)
Significance Pathogenic
Disease Spastic paraplegia 39
Variation info
Gene PNPLA6
CLNDBN Spastic paraplegia 39
Reversed 0
HGVS NC_000019.9:g.7605561G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000087301.6,