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rs558274487

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs558274487(A;A)
Make rs558274487(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position127939952
GeneMFSD8
is asnp
is mentioned by
dbSNPrs558274487
ebirs558274487
HLIrs558274487
Exacrs558274487
Varsomers558274487
Maprs558274487
PheGenIrs558274487
hapmaprs558274487
1000 genomesrs558274487
hgdprs558274487
ensemblrs558274487
gopubmedrs558274487
geneviewrs558274487
scholarrs558274487
googlers558274487
pharmgkbrs558274487
gwascentralrs558274487
openSNPrs558274487
23andMers558274487
23andMe allrs558274487
SNP Nexus

SNPshotrs558274487
SNPdbers558274487
MSV3drs558274487
GWAS Ctlgrs558274487
Max Magnitude0
ClinVar
Risk rs558274487(A;A)
Alt rs558274487(A;A)
Reference rs558274487(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MFSD8
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.128861107C>T
CLNSRC
CLNACC RCV000188167.1,