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rs796052742

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796052742(A;G)
Make rs796052742(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position127942156
GeneMFSD8
is asnp
is mentioned by
dbSNPrs796052742
ebirs796052742
HLIrs796052742
Exacrs796052742
Varsomers796052742
Maprs796052742
PheGenIrs796052742
hapmaprs796052742
1000 genomesrs796052742
hgdprs796052742
ensemblrs796052742
gopubmedrs796052742
geneviewrs796052742
scholarrs796052742
googlers796052742
pharmgkbrs796052742
gwascentralrs796052742
openSNPrs796052742
23andMers796052742
23andMe allrs796052742
SNP Nexus

SNPshotrs796052742
SNPdbers796052742
MSV3drs796052742
GWAS Ctlgrs796052742
Max Magnitude0
ClinVar
Risk rs796052742(G;G)
Alt rs796052742(G;G)
Reference rs796052742(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MFSD8
CLNDBN not provided
Reversed 1
HGVS NC_000004.11:g.128863311T>C
CLNSRC
CLNACC RCV000188168.1,