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rs150802299

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs150802299(A;C)
Make rs150802299(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position530726
GenePIGG
is asnp
is mentioned by
dbSNPrs150802299
dbSNP (old)rs150802299
ClinGenrs150802299
ebirs150802299
HLIrs150802299
Exacrs150802299
Gnomadrs150802299
Varsomers150802299
Maprs150802299
PheGenIrs150802299
Biobankrs150802299
1000 genomesrs150802299
hgdprs150802299
ensemblrs150802299
gopubmedrs150802299
geneviewrs150802299
scholarrs150802299
googlers150802299
pharmgkbrs150802299
gwascentralrs150802299
openSNPrs150802299
23andMers150802299
23andMe allrs150802299
SNPshotrs150802299
SNPdbers150802299
MSV3drs150802299
GWAS Ctlgrs150802299
Max Magnitude0
ClinVar
Risk rs150802299(C;C)
Alt rs150802299(C;C)
Reference Rs150802299(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PIGG
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.524515A>C
CLNSRC
CLNACC RCV000481105.1,