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rs748057401

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs748057401(A;A)
Make rs748057401(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position119493821
GeneHSD17B4
is asnp
is mentioned by
dbSNPrs748057401
dbSNP (classic)rs748057401
ClinGenrs748057401
ebirs748057401
HLIrs748057401
Exacrs748057401
Gnomadrs748057401
Varsomers748057401
LitVarrs748057401
Maprs748057401
PheGenIrs748057401
Biobankrs748057401
1000 genomesrs748057401
hgdprs748057401
ensemblrs748057401
geneviewrs748057401
scholarrs748057401
googlers748057401
pharmgkbrs748057401
gwascentralrs748057401
openSNPrs748057401
23andMers748057401
SNPshotrs748057401
SNPdbers748057401
MSV3drs748057401
GWAS Ctlgrs748057401
Max Magnitude0
ClinVar
Risk rs748057401(A;A)
Alt rs748057401(A;A)
Reference Rs748057401(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene HSD17B4
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.118829516G>A
CLNSRC
CLNACC RCV000493335.1,