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rs751010275

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs751010275(A;C)
Make rs751010275(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position127938843
GeneLOC101927163, MFSD8
is asnp
is mentioned by
dbSNPrs751010275
ebirs751010275
HLIrs751010275
Exacrs751010275
Varsomers751010275
Maprs751010275
PheGenIrs751010275
hapmaprs751010275
1000 genomesrs751010275
hgdprs751010275
ensemblrs751010275
gopubmedrs751010275
geneviewrs751010275
scholarrs751010275
googlers751010275
pharmgkbrs751010275
gwascentralrs751010275
openSNPrs751010275
23andMers751010275
23andMe allrs751010275
SNP Nexus

SNPshotrs751010275
SNPdbers751010275
MSV3drs751010275
GWAS Ctlgrs751010275
Max Magnitude0
ClinVar
Risk rs751010275(C;C)
Alt rs751010275(C;C)
Reference rs751010275(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MFSD8
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.128859998A>C
CLNSRC
CLNACC RCV000188190.1,