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rs797046102

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797046102(G;T)
Make rs797046102(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position49075865
GenePRAF2, WDR45
is asnp
is mentioned by
dbSNPrs797046102
ebirs797046102
HLIrs797046102
Exacrs797046102
Varsomers797046102
Maprs797046102
PheGenIrs797046102
hapmaprs797046102
1000 genomesrs797046102
hgdprs797046102
ensemblrs797046102
gopubmedrs797046102
geneviewrs797046102
scholarrs797046102
googlers797046102
pharmgkbrs797046102
gwascentralrs797046102
openSNPrs797046102
23andMers797046102
23andMe allrs797046102
SNP Nexus

SNPshotrs797046102
SNPdbers797046102
MSV3drs797046102
GWAS Ctlgrs797046102
Max Magnitude0
ClinVar
Risk rs797046102(T;T)
Alt rs797046102(T;T)
Reference rs797046102(G;G)
Significance Pathogenic
Disease Neurodegeneration with brain iron accululation 5
Variation info
Gene WDR45 PRAF2
CLNDBN Neurodegeneration with brain iron accululation 5
Reversed 1
HGVS NC_000023.10:g.48933524C>A
CLNSRC
CLNACC RCV000194153.1,