rs35976361

Orientation

plus

Stabilized

plus

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

Make rs35976361(A;G)

Make rs35976361(G;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

15644736

Gene

BTD

is a	snp
is	mentioned by
dbSNP	rs35976361
dbSNP (classic)	rs35976361
ClinGen	rs35976361
ebi	rs35976361
HLI	rs35976361
Exac	rs35976361
Gnomad	rs35976361
Varsome	rs35976361
LitVar	rs35976361
Map	rs35976361
PheGenI	rs35976361
Biobank	rs35976361
1000 genomes	rs35976361
hgdp	rs35976361
ensembl	rs35976361
geneview	rs35976361
scholar	rs35976361
google	rs35976361
pharmgkb	rs35976361
gwascentral	rs35976361
openSNP	rs35976361
23andMe	rs35976361
SNPshot	rs35976361
SNPdbe	rs35976361
MSV3d	rs35976361
GWAS Ctlg	rs35976361

GMAF

0.01148

Max Magnitude

0

ClinVar
Risk	rs35976361(G;G)
Alt	rs35976361(G;G)
Reference	Rs35976361(A;A)
Significance	Other
Disease	Biotinidase deficiency not provided
Variation	info
Gene	BTD
CLNDBN	Biotinidase deficiency not provided
Reversed	0
HGVS	NC_000003.11:g.15686243A>G
CLNSRC	ARUP BTD
CLNACC	RCV000021969.2, RCV000224487.1,