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rs796052747

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052747(A;A)
Make rs796052747(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position127920749
GeneMFSD8
is asnp
is mentioned by
dbSNPrs796052747
ebirs796052747
HLIrs796052747
Exacrs796052747
Varsomers796052747
Maprs796052747
PheGenIrs796052747
hapmaprs796052747
1000 genomesrs796052747
hgdprs796052747
ensemblrs796052747
gopubmedrs796052747
geneviewrs796052747
scholarrs796052747
googlers796052747
pharmgkbrs796052747
gwascentralrs796052747
openSNPrs796052747
23andMers796052747
23andMe allrs796052747
SNP Nexus

SNPshotrs796052747
SNPdbers796052747
MSV3drs796052747
GWAS Ctlgrs796052747
Max Magnitude0
ClinVar
Risk rs796052747(A;A)
Alt rs796052747(A;A)
Reference rs796052747(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MFSD8
CLNDBN not provided
Reversed 1
HGVS NC_000004.11:g.128841904C>T
CLNSRC
CLNACC RCV000188185.1,