rs267607135

Orientation

minus

Stabilized

minus

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

Make rs267607135(A;A)

Make rs267607135(A;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

137199473

Gene

TPRN

is a	snp
is	mentioned by
dbSNP	rs267607135
dbSNP (classic)	rs267607135
ClinGen	rs267607135
ebi	rs267607135
HLI	rs267607135
Exac	rs267607135
Gnomad	rs267607135
Varsome	rs267607135
LitVar	rs267607135
Map	rs267607135
PheGenI	rs267607135
Biobank	rs267607135
1000 genomes	rs267607135
hgdp	rs267607135
ensembl	rs267607135
geneview	rs267607135
scholar	rs267607135
google	rs267607135
pharmgkb	rs267607135
gwascentral	rs267607135
openSNP	rs267607135
23andMe	rs267607135
SNPshot	rs267607135
SNPdbe	rs267607135
MSV3d	rs267607135
GWAS Ctlg	rs267607135

Max Magnitude

0

ClinVar
Risk	rs267607135(A;A)
Alt	rs267607135(A;A)
Reference	Rs267607135(G;G)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	TPRN
CLNDBN	Deafness, autosomal recessive 79
Reversed	1
HGVS	NC_000009.11:g.140093925C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000000157.2,