Have questions? Visit https://www.reddit.com/r/SNPedia

rs786205574

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205574(C;G)
Make rs786205574(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position119477434
GeneHSD17B4
is asnp
is mentioned by
dbSNPrs786205574
ebirs786205574
HLIrs786205574
Exacrs786205574
Varsomers786205574
Maprs786205574
PheGenIrs786205574
hapmaprs786205574
1000 genomesrs786205574
hgdprs786205574
ensemblrs786205574
gopubmedrs786205574
geneviewrs786205574
scholarrs786205574
googlers786205574
pharmgkbrs786205574
gwascentralrs786205574
openSNPrs786205574
23andMers786205574
23andMe allrs786205574
SNP Nexus

SNPshotrs786205574
SNPdbers786205574
MSV3drs786205574
GWAS Ctlgrs786205574
Max Magnitude0
ClinVar
Risk rs786205574(G;G)
Alt rs786205574(G;G)
Reference rs786205574(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene HSD17B4
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.118813129C>G
CLNSRC
CLNACC RCV000171384.1,