rs876657371

Orientation

plus

Stabilized

plus

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

Make rs876657371(AGCCCAG;C)

Make rs876657371(C;C)

Reference

GRCh38.p2 38.2/147

Chromosome

3

Position

46705788

Gene

TMIE

is a	snp
is	mentioned by
dbSNP	rs876657371
dbSNP (classic)	rs876657371
ClinGen	rs876657371
ebi	rs876657371
HLI	rs876657371
Exac	rs876657371
Gnomad	rs876657371
Varsome	rs876657371
LitVar	rs876657371
Map	rs876657371
PheGenI	rs876657371
Biobank	rs876657371
1000 genomes	rs876657371
hgdp	rs876657371
ensembl	rs876657371
geneview	rs876657371
scholar	rs876657371
google	rs876657371
pharmgkb	rs876657371
gwascentral	rs876657371
openSNP	rs876657371
23andMe	rs876657371
SNPshot	rs876657371
SNPdbe	rs876657371
MSV3d	rs876657371
GWAS Ctlg	rs876657371

Max Magnitude

0

ClinVar
Risk	rs876657371(C;C)
Alt	rs876657371(C;C)
Reference	Rs876657371(AGCCCAG;AGCCCAG)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	TMIE
CLNDBN	Deafness, autosomal recessive 6
Reversed	0
HGVS	NC_000003.11:g.46747278_46747284delAGCCCAGinsC
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003560.4,