rs761389904

Orientation

plus

Stabilized

plus

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

Make rs761389904(G;G)

Make rs761389904(G;T)

Reference

GRCh38.p2 38.2/147

Chromosome

20

Position

13816520

Gene

NDUFAF5

is a	snp
is	mentioned by
dbSNP	rs761389904
dbSNP (classic)	rs761389904
ClinGen	rs761389904
ebi	rs761389904
HLI	rs761389904
Exac	rs761389904
Gnomad	rs761389904
Varsome	rs761389904
LitVar	rs761389904
Map	rs761389904
PheGenI	rs761389904
Biobank	rs761389904
1000 genomes	rs761389904
hgdp	rs761389904
ensembl	rs761389904
geneview	rs761389904
scholar	rs761389904
google	rs761389904
pharmgkb	rs761389904
gwascentral	rs761389904
openSNP	rs761389904
23andMe	rs761389904
SNPshot	rs761389904
SNPdbe	rs761389904
MSV3d	rs761389904
GWAS Ctlg	rs761389904

Max Magnitude

0

ClinVar
Risk	rs761389904(G;G)
Alt	rs761389904(G;G)
Reference	Rs761389904(T;T)
Significance	Probable-Pathogenic
Disease	Inborn genetic diseases
Variation	info
Gene	NDUFAF5
CLNDBN	Inborn genetic diseases
Reversed	0
HGVS	NC_000020.10:g.13797166T>G
CLNSRC
CLNACC	RCV000210569.1,