rs786200883

Orientation

minus

Stabilized

minus

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

Make rs786200883(-;-)

Make rs786200883(-;TTTG)

Reference

GRCh38.p2 38.2/146

Chromosome

15

Position

43614436

Gene

STRC

is a	snp
is	mentioned by
dbSNP	rs786200883
dbSNP (classic)	rs786200883
ClinGen	rs786200883
ebi	rs786200883
HLI	rs786200883
Exac	rs786200883
Gnomad	rs786200883
Varsome	rs786200883
LitVar	rs786200883
Map	rs786200883
PheGenI	rs786200883
Biobank	rs786200883
1000 genomes	rs786200883
hgdp	rs786200883
ensembl	rs786200883
geneview	rs786200883
scholar	rs786200883
google	rs786200883
pharmgkb	rs786200883
gwascentral	rs786200883
openSNP	rs786200883
23andMe	rs786200883
SNPshot	rs786200883
SNPdbe	rs786200883
MSV3d	rs786200883
GWAS Ctlg	rs786200883

Max Magnitude

0

ClinVar
Risk	rs786200883(-;-)
Alt	rs786200883(-;-)
Reference	Rs786200883(TTTG;TTTG)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	STRC
CLNDBN	Deafness, autosomal recessive 16
Reversed	1
HGVS	NC_000015.9:g.43906634_43906637delCAAA
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000004592.3,