rs886043616

Orientation

plus

Stabilized

plus

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

Chromosome

18

Position

46529333

Gene

LOXHD1

is a	snp
is	mentioned by
dbSNP	rs886043616
dbSNP (classic)	rs886043616
ClinGen	rs886043616
ebi	rs886043616
HLI	rs886043616
Exac	rs886043616
Gnomad	rs886043616
Varsome	rs886043616
LitVar	rs886043616
Map	rs886043616
PheGenI	rs886043616
Biobank	rs886043616
1000 genomes	rs886043616
hgdp	rs886043616
ensembl	rs886043616
geneview	rs886043616
scholar	rs886043616
google	rs886043616
pharmgkb	rs886043616
gwascentral	rs886043616
openSNP	rs886043616
23andMe	rs886043616
SNPshot	rs886043616
SNPdbe	rs886043616
MSV3d	rs886043616
GWAS Ctlg	rs886043616

Max Magnitude

0

ClinVar
Risk	rs886043616(C;C)
Alt	rs886043616(C;C)
Reference	Rs886043616(T;T)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	LOXHD1
CLNDBN	Deafness, autosomal recessive 77
Reversed	0
HGVS	NC_000018.9:g.44109296T>C
CLNSRC
CLNACC	RCV000332279.1,