rs75949023

Orientation

plus

Stabilized

plus

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

Make rs75949023(G;T)

Make rs75949023(T;T)

Reference

GRCh38 38.1/141

Chromosome

18

Position

46524734

Gene

LOXHD1

is a	snp
is	mentioned by
dbSNP	rs75949023
dbSNP (classic)	rs75949023
ClinGen	rs75949023
ebi	rs75949023
HLI	rs75949023
Exac	rs75949023
Gnomad	rs75949023
Varsome	rs75949023
LitVar	rs75949023
Map	rs75949023
PheGenI	rs75949023
Biobank	rs75949023
1000 genomes	rs75949023
hgdp	rs75949023
ensembl	rs75949023
geneview	rs75949023
scholar	rs75949023
google	rs75949023
pharmgkb	rs75949023
gwascentral	rs75949023
openSNP	rs75949023
23andMe	rs75949023
SNPshot	rs75949023
SNPdbe	rs75949023
MSV3d	rs75949023
GWAS Ctlg	rs75949023

GMAF

0.02388

Max Magnitude

0

ClinVar
Risk	rs75949023(A;A) rs75949023(T;T)
Alt	rs75949023(A;A) rs75949023(T;T)
Reference	Rs75949023(G;G)
Significance	Pathogenic
Disease	Deafness Nonsyndromic hearing loss and deafness not specified not provided
Variation	info
Gene	LOXHD1
CLNDBN	Deafness, autosomal recessive 77 Nonsyndromic hearing loss and deafness not specified not provided
Reversed	0
HGVS	NC_000018.9:g.44104697G>A; NC_000018.9:g.44104697G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000023981.4, RCV000211793.1, RCV000225012.1, RCV000041212.5, RCV000420867.1,