rs41456348

Orientation

plus

Stabilized

plus

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

Make rs41456348(C;C)

Make rs41456348(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

4336

is a	snp
is	mentioned by
dbSNP	rs41456348
dbSNP (classic)	rs41456348
ClinGen	rs41456348
ebi	rs41456348
HLI	rs41456348
Exac	rs41456348
Gnomad	rs41456348
Varsome	rs41456348
LitVar	rs41456348
Map	rs41456348
PheGenI	rs41456348
Biobank	rs41456348
1000 genomes	rs41456348
hgdp	rs41456348
ensembl	rs41456348
geneview	rs41456348
scholar	rs41456348
google	rs41456348
pharmgkb	rs41456348
gwascentral	rs41456348
openSNP	rs41456348
23andMe	rs41456348
SNPshot	rs41456348
SNPdbe	rs41456348
MSV3d	rs41456348
GWAS Ctlg	rs41456348

Merged from

Rs45517935

GMAF

0.009355

Max Magnitude

0

is a mitochondrial

ClinVar
Risk	rs41456348(C;C)
Alt	rs41456348(C;C)
Reference	Rs41456348(T;T)
Significance	Pathogenic
Disease	Sensorineural deafness and migraine not provided
Variation	info
Gene
CLNDBN	Sensorineural deafness and migraine not provided
Reversed	0
HGVS	NC_012920.1:m.4336T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010239.2, RCV000224964.1,