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rs559155109

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs559155109(A;G)
Make rs559155109(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position127920826
GeneMFSD8
is asnp
is mentioned by
dbSNPrs559155109
dbSNP (classic)rs559155109
ClinGenrs559155109
ebirs559155109
HLIrs559155109
Exacrs559155109
Gnomadrs559155109
Varsomers559155109
LitVarrs559155109
Maprs559155109
PheGenIrs559155109
Biobankrs559155109
1000 genomesrs559155109
hgdprs559155109
ensemblrs559155109
geneviewrs559155109
scholarrs559155109
googlers559155109
pharmgkbrs559155109
gwascentralrs559155109
openSNPrs559155109
23andMers559155109
23andMe allrs559155109
SNPshotrs559155109
SNPdbers559155109
MSV3drs559155109
GWAS Ctlgrs559155109
Max Magnitude0
ClinVar
Risk rs559155109(G;G)
Alt rs559155109(G;G)
Reference Rs559155109(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MFSD8
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.128841981A>G
CLNSRC
CLNACC RCV000480079.1,