rs886037851

Orientation

minus

Stabilized

minus

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

Make rs886037851(A;A)

Make rs886037851(A;G)

Reference

GRCh38.p7 38.3/149

Chromosome

2

Position

171813452

Gene

SLC25A12

is a	snp
is	mentioned by
dbSNP	rs886037851
dbSNP (classic)	rs886037851
ClinGen	rs886037851
ebi	rs886037851
HLI	rs886037851
Exac	rs886037851
Gnomad	rs886037851
Varsome	rs886037851
LitVar	rs886037851
Map	rs886037851
PheGenI	rs886037851
Biobank	rs886037851
1000 genomes	rs886037851
hgdp	rs886037851
ensembl	rs886037851
geneview	rs886037851
scholar	rs886037851
google	rs886037851
pharmgkb	rs886037851
gwascentral	rs886037851
openSNP	rs886037851
23andMe	rs886037851
SNPshot	rs886037851
SNPdbe	rs886037851
MSV3d	rs886037851
GWAS Ctlg	rs886037851

Max Magnitude

0

ClinVar
Risk	rs886037851(A;A)
Alt	rs886037851(A;A)
Reference	Rs886037851(G;G)
Significance	Pathogenic
Disease	Hypomyelination
Variation	info
Gene	SLC25A12
CLNDBN	Hypomyelination, global cerebral
Reversed	1
HGVS	NC_000002.11:g.172669962C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000239515.1,