rs119103280

Orientation

plus

Stabilized

plus

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

Make rs119103280(G;T)

Make rs119103280(T;T)

Reference

GRCh38 38.1/141

Chromosome

19

Position

50244277

Gene

MYH14

is a	snp
is	mentioned by
dbSNP	rs119103280
dbSNP (classic)	rs119103280
ClinGen	rs119103280
ebi	rs119103280
HLI	rs119103280
Exac	rs119103280
Gnomad	rs119103280
Varsome	rs119103280
LitVar	rs119103280
Map	rs119103280
PheGenI	rs119103280
Biobank	rs119103280
1000 genomes	rs119103280
hgdp	rs119103280
ensembl	rs119103280
geneview	rs119103280
scholar	rs119103280
google	rs119103280
pharmgkb	rs119103280
gwascentral	rs119103280
openSNP	rs119103280
23andMe	rs119103280
SNPshot	rs119103280
SNPdbe	rs119103280
MSV3d	rs119103280
GWAS Ctlg	rs119103280

GMAF

0.002755

Max Magnitude

0

OMIM	608568
Desc
Variant	0004
Related	also

ClinVar
Risk	rs119103280(T;T)
Alt	rs119103280(T;T)
Reference	Rs119103280(G;G)
Significance	Pathogenic
Disease	Deafness not specified not provided
Variation	info
Gene	MYH14
CLNDBN	Deafness, autosomal dominant 4 not specified not provided
Reversed	0
HGVS	NC_000019.9:g.50747534G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000002283.3, RCV000037022.4, RCV000438830.1,