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rs796052740

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052740(G;T)
Make rs796052740(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position127965130
GeneABHD18, MFSD8
is asnp
is mentioned by
dbSNPrs796052740
ebirs796052740
HLIrs796052740
Exacrs796052740
Varsomers796052740
Maprs796052740
PheGenIrs796052740
hapmaprs796052740
1000 genomesrs796052740
hgdprs796052740
ensemblrs796052740
gopubmedrs796052740
geneviewrs796052740
scholarrs796052740
googlers796052740
pharmgkbrs796052740
gwascentralrs796052740
openSNPrs796052740
23andMers796052740
23andMe allrs796052740
SNP Nexus

SNPshotrs796052740
SNPdbers796052740
MSV3drs796052740
GWAS Ctlgrs796052740
Max Magnitude0
ClinVar
Risk rs796052740(T;T)
Alt rs796052740(T;T)
Reference rs796052740(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene C4orf29 ABHD18 MFSD8
CLNDBN not provided
Reversed 1
HGVS NC_000004.11:g.128886285C>A
CLNSRC
CLNACC RCV000188161.1,