rs886037927

Orientation

minus

Stabilized

minus

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

Make rs886037927(A;A)

Make rs886037927(A;C)

Reference

GRCh38.p7 38.3/149

Chromosome

X

Position

53431801

Gene

HSD17B10

is a	snp
is	mentioned by
dbSNP	rs886037927
dbSNP (classic)	rs886037927
ClinGen	rs886037927
ebi	rs886037927
HLI	rs886037927
Exac	rs886037927
Gnomad	rs886037927
Varsome	rs886037927
LitVar	rs886037927
Map	rs886037927
PheGenI	rs886037927
Biobank	rs886037927
1000 genomes	rs886037927
hgdp	rs886037927
ensembl	rs886037927
geneview	rs886037927
scholar	rs886037927
google	rs886037927
pharmgkb	rs886037927
gwascentral	rs886037927
openSNP	rs886037927
23andMe	rs886037927
SNPshot	rs886037927
SNPdbe	rs886037927
MSV3d	rs886037927
GWAS Ctlg	rs886037927

Max Magnitude

0

ClinVar
Risk	rs886037927(A;A)
Alt	rs886037927(A;A)
Reference	Rs886037927(C;C)
Significance	Probable-Pathogenic
Disease	2-methyl-3-hydroxybutyric aciduria
Variation	info
Gene	HSD17B10
CLNDBN	2-methyl-3-hydroxybutyric aciduria
Reversed	1
HGVS	NC_000023.10:g.53458749G>T
CLNSRC
CLNACC	RCV000240845.1,