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

rs797044931

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797044931(A;G)
Make rs797044931(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position32327044
GeneHDAC1
is asnp
is mentioned by
dbSNPrs797044931
ebirs797044931
HLIrs797044931
Exacrs797044931
Varsomers797044931
Maprs797044931
PheGenIrs797044931
hapmaprs797044931
1000 genomesrs797044931
hgdprs797044931
ensemblrs797044931
gopubmedrs797044931
geneviewrs797044931
scholarrs797044931
googlers797044931
pharmgkbrs797044931
gwascentralrs797044931
openSNPrs797044931
23andMers797044931
23andMe allrs797044931
SNP Nexus

SNPshotrs797044931
SNPdbers797044931
MSV3drs797044931
GWAS Ctlgrs797044931
Max Magnitude0
ClinVar
Risk rs797044931(G;G)
Alt rs797044931(G;G)
Reference rs797044931(A;A)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene HDAC1
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000001.10:g.32792645A>G
CLNSRC
CLNACC RCV000190771.1,