rs397516421

Orientation

plus

Stabilized

plus

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

Make rs397516421(A;A)

Make rs397516421(A;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

107701101

Gene

SLC26A4

is a	snp
is	mentioned by
dbSNP	rs397516421
dbSNP (classic)	rs397516421
ClinGen	rs397516421
ebi	rs397516421
HLI	rs397516421
Exac	rs397516421
Gnomad	rs397516421
Varsome	rs397516421
LitVar	rs397516421
Map	rs397516421
PheGenI	rs397516421
Biobank	rs397516421
1000 genomes	rs397516421
hgdp	rs397516421
ensembl	rs397516421
geneview	rs397516421
scholar	rs397516421
google	rs397516421
pharmgkb	rs397516421
gwascentral	rs397516421
openSNP	rs397516421
23andMe	rs397516421
SNPshot	rs397516421
SNPdbe	rs397516421
MSV3d	rs397516421
GWAS Ctlg	rs397516421

Max Magnitude

0

ClinVar
Risk	rs397516421(A;A)
Alt	rs397516421(A;A)
Reference	Rs397516421(G;G)
Significance	Probable-Pathogenic
Disease	not specified
Variation	info
Gene	SLC26A4
CLNDBN	not specified
Reversed	0
HGVS	NC_000007.13:g.107341546G>A
CLNSRC	ClinVar
CLNACC	RCV000036456.3,