rs104894528

Orientation

plus

Stabilized

plus

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

Make rs104894528(C;G)

Make rs104894528(G;G)

Reference

GRCh38 38.1/141

Chromosome

16

Position

83907018

Gene

MLYCD

is a	snp
is	mentioned by
dbSNP	rs104894528
dbSNP (classic)	rs104894528
ClinGen	rs104894528
ebi	rs104894528
HLI	rs104894528
Exac	rs104894528
Gnomad	rs104894528
Varsome	rs104894528
LitVar	rs104894528
Map	rs104894528
PheGenI	rs104894528
Biobank	rs104894528
1000 genomes	rs104894528
hgdp	rs104894528
ensembl	rs104894528
geneview	rs104894528
scholar	rs104894528
google	rs104894528
pharmgkb	rs104894528
gwascentral	rs104894528
openSNP	rs104894528
23andMe	rs104894528
SNPshot	rs104894528
SNPdbe	rs104894528
MSV3d	rs104894528
GWAS Ctlg	rs104894528

Max Magnitude

0

OMIM	606761
Desc
Variant	0001
Related	also

ClinVar
Risk	rs104894528(G;G)
Alt	rs104894528(G;G)
Reference	Rs104894528(C;C)
Significance	Pathogenic
Disease	Deficiency of malonyl-CoA decarboxylase
Variation	info
Gene	MLYCD
CLNDBN	Deficiency of malonyl-CoA decarboxylase
Reversed	0
HGVS	NC_000016.9:g.83940623C>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000004270.2,