rs387906222

Orientation

minus

Stabilized

minus

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

Make rs387906222(-;-)

Make rs387906222(-;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

137199182

Gene

TPRN

is a	snp
is	mentioned by
dbSNP	rs387906222
dbSNP (classic)	rs387906222
ClinGen	rs387906222
ebi	rs387906222
HLI	rs387906222
Exac	rs387906222
Gnomad	rs387906222
Varsome	rs387906222
LitVar	rs387906222
Map	rs387906222
PheGenI	rs387906222
Biobank	rs387906222
1000 genomes	rs387906222
hgdp	rs387906222
ensembl	rs387906222
geneview	rs387906222
scholar	rs387906222
google	rs387906222
pharmgkb	rs387906222
gwascentral	rs387906222
openSNP	rs387906222
23andMe	rs387906222
SNPshot	rs387906222
SNPdbe	rs387906222
MSV3d	rs387906222
GWAS Ctlg	rs387906222

Max Magnitude

0

ClinVar
Risk	rs387906222(-;-)
Alt	rs387906222(-;-)
Reference	Rs387906222(G;G)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	TPRN
CLNDBN	Deafness, autosomal recessive 79
Reversed	1
HGVS	NC_000009.11:g.140093634delC
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000000161.3,