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rs863225241

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863225241(A;A)
Make rs863225241(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position155317996
GeneFDPS, LOC105371451
is asnp
is mentioned by
dbSNPrs863225241
ebirs863225241
HLIrs863225241
Exacrs863225241
Varsomers863225241
Maprs863225241
PheGenIrs863225241
hapmaprs863225241
1000 genomesrs863225241
hgdprs863225241
ensemblrs863225241
gopubmedrs863225241
geneviewrs863225241
scholarrs863225241
googlers863225241
pharmgkbrs863225241
gwascentralrs863225241
openSNPrs863225241
23andMers863225241
23andMe allrs863225241
SNP Nexus

SNPshotrs863225241
SNPdbers863225241
MSV3drs863225241
GWAS Ctlgrs863225241
Max Magnitude0
ClinVar
Risk rs863225241(A;A)
Alt rs863225241(A;A)
Reference rs863225241(G;G)
Significance Pathogenic
Disease Porokeratosis 9
Variation info
Gene FDPS
CLNDBN Porokeratosis 9, multiple types
Reversed 0
HGVS NC_000001.10:g.155287787G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000201791.3,