rs796053287

Orientation

plus

Stabilized

plus

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

Make rs796053287(C;C)

Make rs796053287(C;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

136040093

Gene

SLC9A6

is a	snp
is	mentioned by
dbSNP	rs796053287
dbSNP (classic)	rs796053287
ClinGen	rs796053287
ebi	rs796053287
HLI	rs796053287
Exac	rs796053287
Gnomad	rs796053287
Varsome	rs796053287
LitVar	rs796053287
Map	rs796053287
PheGenI	rs796053287
Biobank	rs796053287
1000 genomes	rs796053287
hgdp	rs796053287
ensembl	rs796053287
geneview	rs796053287
scholar	rs796053287
google	rs796053287
pharmgkb	rs796053287
gwascentral	rs796053287
openSNP	rs796053287
23andMe	rs796053287
SNPshot	rs796053287
SNPdbe	rs796053287
MSV3d	rs796053287
GWAS Ctlg	rs796053287

Max Magnitude

0

ClinVar
Risk	rs796053287(C;C)
Alt	rs796053287(C;C)
Reference	Rs796053287(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SLC9A6
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.135122252T>C
CLNSRC
CLNACC	RCV000189414.2,