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rs796051979

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796051979(A;A)
Make rs796051979(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position119759862
GeneHMGCS2
is asnp
is mentioned by
dbSNPrs796051979
ebirs796051979
HLIrs796051979
Exacrs796051979
Varsomers796051979
Maprs796051979
PheGenIrs796051979
hapmaprs796051979
1000 genomesrs796051979
hgdprs796051979
ensemblrs796051979
gopubmedrs796051979
geneviewrs796051979
scholarrs796051979
googlers796051979
pharmgkbrs796051979
gwascentralrs796051979
openSNPrs796051979
23andMers796051979
23andMe allrs796051979
SNP Nexus

SNPshotrs796051979
SNPdbers796051979
MSV3drs796051979
GWAS Ctlgrs796051979
Max Magnitude0
ClinVar
Risk rs796051979(A;A)
Alt rs796051979(A;A)
Reference rs796051979(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene HMGCS2
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.120302485A>T
CLNSRC
CLNACC RCV000185974.2,