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rs1057518388

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057518388(A;G)
Make rs1057518388(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position127920838
GeneMFSD8
is asnp
is mentioned by
dbSNPrs1057518388
dbSNP (old)rs1057518388
ClinGenrs1057518388
ebirs1057518388
HLIrs1057518388
Exacrs1057518388
Gnomadrs1057518388
Varsomers1057518388
Maprs1057518388
PheGenIrs1057518388
Biobankrs1057518388
1000 genomesrs1057518388
hgdprs1057518388
ensemblrs1057518388
gopubmedrs1057518388
geneviewrs1057518388
scholarrs1057518388
googlers1057518388
pharmgkbrs1057518388
gwascentralrs1057518388
openSNPrs1057518388
23andMers1057518388
23andMe allrs1057518388
SNPshotrs1057518388
SNPdbers1057518388
MSV3drs1057518388
GWAS Ctlgrs1057518388
Max Magnitude0
ClinVar
Risk rs1057518388(G;G)
Alt rs1057518388(G;G)
Reference Rs1057518388(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MFSD8
CLNDBN not provided
Reversed 1
HGVS NC_000004.11:g.128841993T>C
CLNSRC
CLNACC RCV000413554.1,