rs776631396

Orientation

plus

Stabilized

plus

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

Make rs776631396(C;T)

Make rs776631396(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

6

Position

80167744

Gene

BCKDHB

is a	snp
is	mentioned by
dbSNP	rs776631396
dbSNP (classic)	rs776631396
ClinGen	rs776631396
ebi	rs776631396
HLI	rs776631396
Exac	rs776631396
Gnomad	rs776631396
Varsome	rs776631396
LitVar	rs776631396
Map	rs776631396
PheGenI	rs776631396
Biobank	rs776631396
1000 genomes	rs776631396
hgdp	rs776631396
ensembl	rs776631396
geneview	rs776631396
scholar	rs776631396
google	rs776631396
pharmgkb	rs776631396
gwascentral	rs776631396
openSNP	rs776631396
23andMe	rs776631396
SNPshot	rs776631396
SNPdbe	rs776631396
MSV3d	rs776631396
GWAS Ctlg	rs776631396

Max Magnitude

0

ClinVar
Risk	rs776631396(T;T)
Alt	rs776631396(T;T)
Reference	Rs776631396(C;C)
Significance	Probable-Pathogenic
Disease	Maple syrup urine disease
Variation	info
Gene	BCKDHB
CLNDBN	Maple syrup urine disease
Reversed	0
HGVS	NC_000006.11:g.80877461C>T
CLNSRC
CLNACC	RCV000410485.1,