rs876661405

Orientation

plus

Stabilized

plus

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

Make rs876661405(A;A)

Make rs876661405(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

19

Position

44704140

Gene	CEACAM16, LOC107985305

is a	snp
is	mentioned by
dbSNP	rs876661405
dbSNP (classic)	rs876661405
ClinGen	rs876661405
ebi	rs876661405
HLI	rs876661405
Exac	rs876661405
Gnomad	rs876661405
Varsome	rs876661405
LitVar	rs876661405
Map	rs876661405
PheGenI	rs876661405
Biobank	rs876661405
1000 genomes	rs876661405
hgdp	rs876661405
ensembl	rs876661405
geneview	rs876661405
scholar	rs876661405
google	rs876661405
pharmgkb	rs876661405
gwascentral	rs876661405
openSNP	rs876661405
23andMe	rs876661405
SNPshot	rs876661405
SNPdbe	rs876661405
MSV3d	rs876661405
GWAS Ctlg	rs876661405

Max Magnitude

0

ClinVar
Risk	rs876661405(A;A)
Alt	rs876661405(A;A)
Reference	Rs876661405(G;G)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	CEACAM16
CLNDBN	Deafness, autosomal dominant 4b
Reversed	0
HGVS	NC_000019.9:g.45207410G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000223943.2,