rs140236996

Orientation

plus

Stabilized

plus

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

Make rs140236996(C;T)

Make rs140236996(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

121168064

Gene

TECTA

is a	snp
is	mentioned by
dbSNP	rs140236996
dbSNP (classic)	rs140236996
ClinGen	rs140236996
ebi	rs140236996
HLI	rs140236996
Exac	rs140236996
Gnomad	rs140236996
Varsome	rs140236996
LitVar	rs140236996
Map	rs140236996
PheGenI	rs140236996
Biobank	rs140236996
1000 genomes	rs140236996
hgdp	rs140236996
ensembl	rs140236996
geneview	rs140236996
scholar	rs140236996
google	rs140236996
pharmgkb	rs140236996
gwascentral	rs140236996
openSNP	rs140236996
23andMe	rs140236996
SNPshot	rs140236996
SNPdbe	rs140236996
MSV3d	rs140236996
GWAS Ctlg	rs140236996

Max Magnitude

0

ClinVar
Risk	rs140236996(G;G) rs140236996(T;T)
Alt	rs140236996(G;G) rs140236996(T;T)
Reference	Rs140236996(C;C)
Significance	Pathogenic
Disease	Deafness Nonsyndromic Hearing Loss Nonsyndromic Hearing Loss not provided
Variation	info
Gene	TECTA
CLNDBN	Deafness, autosomal dominant 12 Nonsyndromic Hearing Loss, Recessive Nonsyndromic Hearing Loss, Dominant not provided
Reversed	0
HGVS	NC_000011.9:g.121038773C>T
CLNSRC
CLNACC	RCV000225064.2, RCV000264805.1, RCV000324612.1, RCV000479439.1,