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rs1060502664

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060502664(-;-)
Make rs1060502664(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position7561219
GenePNPLA6
is asnp
is mentioned by
dbSNPrs1060502664
dbSNP (classic)rs1060502664
ClinGenrs1060502664
ebirs1060502664
HLIrs1060502664
Exacrs1060502664
Gnomadrs1060502664
Varsomers1060502664
LitVarrs1060502664
Maprs1060502664
PheGenIrs1060502664
Biobankrs1060502664
1000 genomesrs1060502664
hgdprs1060502664
ensemblrs1060502664
geneviewrs1060502664
scholarrs1060502664
googlers1060502664
pharmgkbrs1060502664
gwascentralrs1060502664
openSNPrs1060502664
23andMers1060502664
23andMe allrs1060502664
SNPshotrs1060502664
SNPdbers1060502664
MSV3drs1060502664
GWAS Ctlgrs1060502664
Max Magnitude0
ClinVar
Risk rs1060502664(-;-)
Alt rs1060502664(-;-)
Reference Rs1060502664(G;G)
Significance Pathogenic
Disease Spastic paraplegia 39
Variation info
Gene PNPLA6
CLNDBN Spastic paraplegia 39
Reversed 0
HGVS NC_000019.9:g.7626105delG
CLNSRC
CLNACC RCV000462018.1,