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rs796052752

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs796052752(-;-)
Make rs796052752(-;A)
Make rs796052752(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position127943973
GeneMFSD8
is asnp
is mentioned by
dbSNPrs796052752
ebirs796052752
HLIrs796052752
Exacrs796052752
Varsomers796052752
Maprs796052752
PheGenIrs796052752
hapmaprs796052752
1000 genomesrs796052752
hgdprs796052752
ensemblrs796052752
gopubmedrs796052752
geneviewrs796052752
scholarrs796052752
googlers796052752
pharmgkbrs796052752
gwascentralrs796052752
openSNPrs796052752
23andMers796052752
23andMe allrs796052752
SNP Nexus

SNPshotrs796052752
SNPdbers796052752
MSV3drs796052752
GWAS Ctlgrs796052752
Max Magnitude0
ClinVar
Risk rs796052752(A;A)
Alt rs796052752(A;A)
Reference rs796052752(;)
Significance Pathogenic
Disease not provided
Variation info
Gene MFSD8
CLNDBN not provided
Reversed 1
HGVS NC_000004.11:g.128865129dupT
CLNSRC
CLNACC RCV000188195.1,