rs41362547

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common on affy axiom data

Make rs41362547(A;G)

Make rs41362547(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

10044

is a	snp
is	mentioned by
dbSNP	rs41362547
dbSNP (classic)	rs41362547
ClinGen	rs41362547
ebi	rs41362547
HLI	rs41362547
Exac	rs41362547
Gnomad	rs41362547
Varsome	rs41362547
LitVar	rs41362547
Map	rs41362547
PheGenI	rs41362547
Biobank	rs41362547
1000 genomes	rs41362547
hgdp	rs41362547
ensembl	rs41362547
geneview	rs41362547
scholar	rs41362547
google	rs41362547
pharmgkb	rs41362547
gwascentral	rs41362547
openSNP	rs41362547
23andMe	rs41362547
SNPshot	rs41362547
SNPdbe	rs41362547
MSV3d	rs41362547
GWAS Ctlg	rs41362547

GMAF

0.003742

Max Magnitude

0

haplogroups

ClinVar
Risk	rs41362547(G;G)
Alt	rs41362547(G;G)
Reference	Rs41362547(A;A)
Significance	Pathogenic
Disease	Sudden death
Variation	info
Gene
CLNDBN	Sudden death
Reversed	0
HGVS	NC_012920.1:m.10044A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010237.2,