rs201632198

Orientation

plus

Stabilized

plus

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

Make rs201632198(A;A)

Make rs201632198(A;G)

Reference

GRCh38 38.1/141

Chromosome

21

Position

42388524

Gene

TMPRSS3

is a	snp
is	mentioned by
dbSNP	rs201632198
dbSNP (classic)	rs201632198
ClinGen	rs201632198
ebi	rs201632198
HLI	rs201632198
Exac	rs201632198
Gnomad	rs201632198
Varsome	rs201632198
LitVar	rs201632198
Map	rs201632198
PheGenI	rs201632198
Biobank	rs201632198
1000 genomes	rs201632198
hgdp	rs201632198
ensembl	rs201632198
geneview	rs201632198
scholar	rs201632198
google	rs201632198
pharmgkb	rs201632198
gwascentral	rs201632198
openSNP	rs201632198
23andMe	rs201632198
SNPshot	rs201632198
SNPdbe	rs201632198
MSV3d	rs201632198
GWAS Ctlg	rs201632198

Max Magnitude

0

ClinVar
Risk	rs201632198(A;A)
Alt	rs201632198(A;A)
Reference	Rs201632198(G;G)
Significance	Pathogenic
Disease	Deafness Nonsyndromic hearing loss and deafness Nonsyndromic Hearing Loss not provided
Variation	info
Gene	TMPRSS3
CLNDBN	Deafness, autosomal recessive 8 Nonsyndromic hearing loss and deafness Nonsyndromic Hearing Loss, Recessive not provided
Reversed	0
HGVS	NC_000021.8:g.43808633G>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000039351.4, RCV000211860.1, RCV000262015.1, RCV000332878.1,