rs200607527

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs200607527(A;A)

Make rs200607527(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

119764385

Gene

HMGCS2

is a	snp
is	mentioned by
dbSNP	rs200607527
dbSNP (classic)	rs200607527
ClinGen	rs200607527
ebi	rs200607527
HLI	rs200607527
Exac	rs200607527
Gnomad	rs200607527
Varsome	rs200607527
LitVar	rs200607527
Map	rs200607527
PheGenI	rs200607527
Biobank	rs200607527
1000 genomes	rs200607527
hgdp	rs200607527
ensembl	rs200607527
geneview	rs200607527
scholar	rs200607527
google	rs200607527
pharmgkb	rs200607527
gwascentral	rs200607527
openSNP	rs200607527
23andMe	rs200607527
SNPshot	rs200607527
SNPdbe	rs200607527
MSV3d	rs200607527
GWAS Ctlg	rs200607527

Max Magnitude

0

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,