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rs1057519212

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CA;CA) 0 common in clinvar
Make rs1057519212(-;-)
Make rs1057519212(-;CA)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position119541962
GeneHSD17B4
is asnp
is mentioned by
dbSNPrs1057519212
dbSNP (classic)rs1057519212
ClinGenrs1057519212
ebirs1057519212
HLIrs1057519212
Exacrs1057519212
Gnomadrs1057519212
Varsomers1057519212
LitVarrs1057519212
Maprs1057519212
PheGenIrs1057519212
Biobankrs1057519212
1000 genomesrs1057519212
hgdprs1057519212
ensemblrs1057519212
geneviewrs1057519212
scholarrs1057519212
googlers1057519212
pharmgkbrs1057519212
gwascentralrs1057519212
openSNPrs1057519212
23andMers1057519212
23andMe allrs1057519212
SNPshotrs1057519212
SNPdbers1057519212
MSV3drs1057519212
GWAS Ctlgrs1057519212
Max Magnitude0
ClinVar
Risk rs1057519212(-;-)
Alt rs1057519212(-;-)
Reference Rs1057519212(CA;CA)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene HSD17B4
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.118877657_118877658delCA
CLNSRC
CLNACC RCV000415984.2,