rs28937908

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	1	no call
(T;T)	0	common in clinvar

Make rs28937908(C;C)

Make rs28937908(C;T)

Reference

GRCh38 38.1/141

Chromosome

16

Position

83899263

Gene

MLYCD

is a	snp
is	mentioned by
dbSNP	rs28937908
dbSNP (classic)	rs28937908
ClinGen	rs28937908
ebi	rs28937908
HLI	rs28937908
Exac	rs28937908
Gnomad	rs28937908
Varsome	rs28937908
LitVar	rs28937908
Map	rs28937908
PheGenI	rs28937908
Biobank	rs28937908
1000 genomes	rs28937908
hgdp	rs28937908
ensembl	rs28937908
geneview	rs28937908
scholar	rs28937908
google	rs28937908
pharmgkb	rs28937908
gwascentral	rs28937908
openSNP	rs28937908
23andMe	rs28937908
SNPshot	rs28937908
SNPdbe	rs28937908
MSV3d	rs28937908
GWAS Ctlg	rs28937908

Max Magnitude

1

OMIM	606761
Desc	MALONYL-CoA DECARBOXYLASE DEFICIENCY
Variant	0006
Related	also

ClinVar
Risk	rs28937908(C;C)
Alt	rs28937908(C;C)
Reference	Rs28937908(T;T)
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.83932868T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000004275.2,