rs876657776

Orientation

minus

Stabilized

minus

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

Make rs876657776(C;T)

Make rs876657776(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

5

Position

141524167

Gene

DIAPH1

is a	snp
is	mentioned by
dbSNP	rs876657776
dbSNP (classic)	rs876657776
ClinGen	rs876657776
ebi	rs876657776
HLI	rs876657776
Exac	rs876657776
Gnomad	rs876657776
Varsome	rs876657776
LitVar	rs876657776
Map	rs876657776
PheGenI	rs876657776
Biobank	rs876657776
1000 genomes	rs876657776
hgdp	rs876657776
ensembl	rs876657776
geneview	rs876657776
scholar	rs876657776
google	rs876657776
pharmgkb	rs876657776
gwascentral	rs876657776
openSNP	rs876657776
23andMe	rs876657776
SNPshot	rs876657776
SNPdbe	rs876657776
MSV3d	rs876657776
GWAS Ctlg	rs876657776

Max Magnitude

0

ClinVar
Risk	rs876657776(T;T)
Alt	rs876657776(T;T)
Reference	Rs876657776(C;C)
Significance	Pathogenic
Disease	not specified Deafness
Variation	info
Gene	DIAPH1
CLNDBN	not specified Deafness, autosomal dominant 1
Reversed	1
HGVS	NC_000005.9:g.140903734G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000216048.1, RCV000488049.1,