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

rs775766910

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs775766910(A;C)
Make rs775766910(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position119478925
GeneHSD17B4
is asnp
is mentioned by
dbSNPrs775766910
ebirs775766910
HLIrs775766910
Exacrs775766910
Varsomers775766910
Maprs775766910
PheGenIrs775766910
hapmaprs775766910
1000 genomesrs775766910
hgdprs775766910
ensemblrs775766910
gopubmedrs775766910
geneviewrs775766910
scholarrs775766910
googlers775766910
pharmgkbrs775766910
gwascentralrs775766910
openSNPrs775766910
23andMers775766910
23andMe allrs775766910
SNP Nexus

SNPshotrs775766910
SNPdbers775766910
MSV3drs775766910
GWAS Ctlgrs775766910
Max Magnitude0
ClinVar
Risk rs775766910(C;C)
Alt rs775766910(C;C)
Reference rs775766910(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene HSD17B4
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.118814620A>G
CLNSRC
CLNACC RCV000171385.1,