rs483352866

Orientation

plus

Stabilized

plus

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

Make rs483352866(C;T)

Make rs483352866(T;T)

Reference

GRCh38 38.1/142

Chromosome

16

Position

2496681

Gene

TBC1D24

is a	snp
is	mentioned by
dbSNP	rs483352866
dbSNP (classic)	rs483352866
ClinGen	rs483352866
ebi	rs483352866
HLI	rs483352866
Exac	rs483352866
Gnomad	rs483352866
Varsome	rs483352866
LitVar	rs483352866
Map	rs483352866
PheGenI	rs483352866
Biobank	rs483352866
1000 genomes	rs483352866
hgdp	rs483352866
ensembl	rs483352866
geneview	rs483352866
scholar	rs483352866
google	rs483352866
pharmgkb	rs483352866
gwascentral	rs483352866
openSNP	rs483352866
23andMe	rs483352866
SNPshot	rs483352866
SNPdbe	rs483352866
MSV3d	rs483352866
GWAS Ctlg	rs483352866

Max Magnitude

0

ClinVar
Risk	rs483352866(T;T)
Alt	rs483352866(T;T)
Reference	Rs483352866(C;C)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	TBC1D24
CLNDBN	Deafness, autosomal recessive 86 Deafness, autosomal dominant 65
Reversed	0
HGVS	NC_000016.9:g.2546682C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000119776.1, RCV000144534.2,