Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1057519420

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CAGAT;CAGAT) 0 common in clinvar
Make rs1057519420(AAA;AAA)
Make rs1057519420(AAA;CAGAT)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position119541962
GeneHSD17B4
is asnp
is mentioned by
dbSNPrs1057519420
dbSNP (old)rs1057519420
ClinGenrs1057519420
ebirs1057519420
HLIrs1057519420
Exacrs1057519420
Gnomadrs1057519420
Varsomers1057519420
Maprs1057519420
PheGenIrs1057519420
Biobankrs1057519420
1000 genomesrs1057519420
hgdprs1057519420
ensemblrs1057519420
gopubmedrs1057519420
geneviewrs1057519420
scholarrs1057519420
googlers1057519420
pharmgkbrs1057519420
gwascentralrs1057519420
openSNPrs1057519420
23andMers1057519420
23andMe allrs1057519420
SNPshotrs1057519420
SNPdbers1057519420
MSV3drs1057519420
GWAS Ctlgrs1057519420
Max Magnitude0
ClinVar
Risk rs1057519420(AAA;AAA)
Alt rs1057519420(AAA;AAA)
Reference Rs1057519420(CAGAT;CAGAT)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene HSD17B4
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.118877657_118877661delinsAAA
CLNSRC
CLNACC RCV000415947.1,