rs119103281

Orientation

plus

Stabilized

plus

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

Make rs119103281(C;T)

Make rs119103281(T;T)

Reference

GRCh38 38.1/141

Chromosome

19

Position

50210724

Gene

MYH14

is a	snp
is	mentioned by
dbSNP	rs119103281
dbSNP (classic)	rs119103281
ClinGen	rs119103281
ebi	rs119103281
HLI	rs119103281
Exac	rs119103281
Gnomad	rs119103281
Varsome	rs119103281
LitVar	rs119103281
Map	rs119103281
PheGenI	rs119103281
Biobank	rs119103281
1000 genomes	rs119103281
hgdp	rs119103281
ensembl	rs119103281
geneview	rs119103281
scholar	rs119103281
google	rs119103281
pharmgkb	rs119103281
gwascentral	rs119103281
openSNP	rs119103281
23andMe	rs119103281
SNPshot	rs119103281
SNPdbe	rs119103281
MSV3d	rs119103281
GWAS Ctlg	rs119103281

Max Magnitude

0

OMIM	608568
Desc
Variant	0005
Related	also

ClinVar
Risk	rs119103281(T;T)
Alt	rs119103281(T;T)
Reference	Rs119103281(C;C)
Significance	Pathogenic
Disease	Deafness not provided
Variation	info
Gene	MYH14
CLNDBN	Deafness, autosomal dominant 4 not provided
Reversed	0
HGVS	NC_000019.9:g.50713981C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000002284.4, RCV000481506.1,