rs207460003

Orientation

plus

Stabilized

plus

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

Make rs207460003(A;A)

Make rs207460003(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

15498

Gene

CYTB

is a	snp
is	mentioned by
dbSNP	rs207460003
dbSNP (classic)	rs207460003
ClinGen	rs207460003
ebi	rs207460003
HLI	rs207460003
Exac	rs207460003
Gnomad	rs207460003
Varsome	rs207460003
LitVar	rs207460003
Map	rs207460003
PheGenI	rs207460003
Biobank	rs207460003
1000 genomes	rs207460003
hgdp	rs207460003
ensembl	rs207460003
geneview	rs207460003
scholar	rs207460003
google	rs207460003
pharmgkb	rs207460003
gwascentral	rs207460003
openSNP	rs207460003
23andMe	rs207460003
SNPshot	rs207460003
SNPdbe	rs207460003
MSV3d	rs207460003
GWAS Ctlg	rs207460003

Max Magnitude

0

ClinVar
Risk	rs207460003(A;A)
Alt	rs207460003(A;A)
Reference	Rs207460003(G;G)
Significance	Pathogenic
Disease	Infantile histiocytoid cardiomyopathy
Variation	info
Gene	CYTB
CLNDBN	Infantile histiocytoid cardiomyopathy
Reversed	0
HGVS	NC_012920.1:m.15498G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010322.2,