rs886039425

Orientation

minus

Stabilized

minus

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

Make rs886039425(C;T)

Make rs886039425(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

2

Position

149576443

Gene

MMADHC

is a	snp
is	mentioned by
dbSNP	rs886039425
dbSNP (classic)	rs886039425
ClinGen	rs886039425
ebi	rs886039425
HLI	rs886039425
Exac	rs886039425
Gnomad	rs886039425
Varsome	rs886039425
LitVar	rs886039425
Map	rs886039425
PheGenI	rs886039425
Biobank	rs886039425
1000 genomes	rs886039425
hgdp	rs886039425
ensembl	rs886039425
geneview	rs886039425
scholar	rs886039425
google	rs886039425
pharmgkb	rs886039425
gwascentral	rs886039425
openSNP	rs886039425
23andMe	rs886039425
SNPshot	rs886039425
SNPdbe	rs886039425
MSV3d	rs886039425
GWAS Ctlg	rs886039425

Max Magnitude

0

ClinVar
Risk	rs886039425(T;T)
Alt	rs886039425(T;T)
Reference	Rs886039425(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MMADHC
CLNDBN	not provided
Reversed	1
HGVS	NC_000002.11:g.150432957G>A
CLNSRC
CLNACC	RCV000255676.1,