rs549522925

Orientation

plus

Stabilized

plus

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

Make rs549522925(A;A)

Make rs549522925(A;C)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

149582208

Gene

MMADHC

is a	snp
is	mentioned by
dbSNP	rs549522925
dbSNP (classic)	rs549522925
ClinGen	rs549522925
ebi	rs549522925
HLI	rs549522925
Exac	rs549522925
Gnomad	rs549522925
Varsome	rs549522925
LitVar	rs549522925
Map	rs549522925
PheGenI	rs549522925
Biobank	rs549522925
1000 genomes	rs549522925
hgdp	rs549522925
ensembl	rs549522925
geneview	rs549522925
scholar	rs549522925
google	rs549522925
pharmgkb	rs549522925
gwascentral	rs549522925
openSNP	rs549522925
23andMe	rs549522925
SNPshot	rs549522925
SNPdbe	rs549522925
MSV3d	rs549522925
GWAS Ctlg	rs549522925

Max Magnitude

0

ClinVar
Risk	rs549522925(A;A) rs549522925(G;G)
Alt	rs549522925(A;A) rs549522925(G;G)
Reference	Rs549522925(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MMADHC
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.150438722C>A
CLNSRC
CLNACC	RCV000186038.1,