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rs200607527

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs200607527(A;A)
Make rs200607527(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position119764385
GeneHMGCS2
is asnp
is mentioned by
dbSNPrs200607527
dbSNP (old)rs200607527
ClinGenrs200607527
ebirs200607527
HLIrs200607527
Exacrs200607527
Gnomadrs200607527
Varsomers200607527
Maprs200607527
PheGenIrs200607527
Biobankrs200607527
1000 genomesrs200607527
hgdprs200607527
ensemblrs200607527
gopubmedrs200607527
geneviewrs200607527
scholarrs200607527
googlers200607527
pharmgkbrs200607527
gwascentralrs200607527
openSNPrs200607527
23andMers200607527
23andMe allrs200607527
SNP Nexus

SNPshotrs200607527
SNPdbers200607527
MSV3drs200607527
GWAS Ctlgrs200607527
Max Magnitude0
ClinVar
Risk rs200607527(A;A)
Alt rs200607527(A;A)
Reference Rs200607527(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene HMGCS2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.120307008G>A
CLNSRC
CLNACC RCV000185972.1,