rs778909195

Orientation

plus

Stabilized

plus

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

Make rs778909195(A;A)

Make rs778909195(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

15

Position

43604020

Gene

STRC

is a	snp
is	mentioned by
dbSNP	rs778909195
dbSNP (classic)	rs778909195
ClinGen	rs778909195
ebi	rs778909195
HLI	rs778909195
Exac	rs778909195
Gnomad	rs778909195
Varsome	rs778909195
LitVar	rs778909195
Map	rs778909195
PheGenI	rs778909195
Biobank	rs778909195
1000 genomes	rs778909195
hgdp	rs778909195
ensembl	rs778909195
geneview	rs778909195
scholar	rs778909195
google	rs778909195
pharmgkb	rs778909195
gwascentral	rs778909195
openSNP	rs778909195
23andMe	rs778909195
SNPshot	rs778909195
SNPdbe	rs778909195
MSV3d	rs778909195
GWAS Ctlg	rs778909195

Max Magnitude

0

ClinVar
Risk	rs778909195(A;A)
Alt	rs778909195(A;A)
Reference	Rs778909195(G;G)
Significance	Probable-Pathogenic
Disease	Deafness
Variation	info
Gene	STRC
CLNDBN	Deafness, autosomal recessive 16
Reversed	0
HGVS	NC_000015.9:g.43896218G>A
CLNSRC
CLNACC	RCV000193949.1,