rs1057518810

Orientation

plus

Stabilized

plus

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

Make rs1057518810(C;C)

Make rs1057518810(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

107663430

Gene	SLC26A4, SLC26A4-AS1

is a	snp
is	mentioned by
dbSNP	rs1057518810
dbSNP (classic)	rs1057518810
ClinGen	rs1057518810
ebi	rs1057518810
HLI	rs1057518810
Exac	rs1057518810
Gnomad	rs1057518810
Varsome	rs1057518810
LitVar	rs1057518810
Map	rs1057518810
PheGenI	rs1057518810
Biobank	rs1057518810
1000 genomes	rs1057518810
hgdp	rs1057518810
ensembl	rs1057518810
geneview	rs1057518810
scholar	rs1057518810
google	rs1057518810
pharmgkb	rs1057518810
gwascentral	rs1057518810
openSNP	rs1057518810
23andMe	rs1057518810
SNPshot	rs1057518810
SNPdbe	rs1057518810
MSV3d	rs1057518810
GWAS Ctlg	rs1057518810

Max Magnitude

0

ClinVar
Risk	rs1057518810(C;C)
Alt	rs1057518810(C;C)
Reference	Rs1057518810(T;T)
Significance	Probable-Pathogenic
Disease	Hearing impairment
Variation	info
Gene	SLC26A4-AS1 SLC26A4
CLNDBN	Hearing impairment
Reversed	0
HGVS	NC_000007.13:g.107303875T>C
CLNSRC
CLNACC	RCV000414878.1,