rs122461162

Orientation

plus

Stabilized

plus

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

Make rs122461162(C;T)

Make rs122461162(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

136024365

Gene

SLC9A6

is a	snp
is	mentioned by
dbSNP	rs122461162
dbSNP (classic)	rs122461162
ClinGen	rs122461162
ebi	rs122461162
HLI	rs122461162
Exac	rs122461162
Gnomad	rs122461162
Varsome	rs122461162
LitVar	rs122461162
Map	rs122461162
PheGenI	rs122461162
Biobank	rs122461162
1000 genomes	rs122461162
hgdp	rs122461162
ensembl	rs122461162
geneview	rs122461162
scholar	rs122461162
google	rs122461162
pharmgkb	rs122461162
gwascentral	rs122461162
openSNP	rs122461162
23andMe	rs122461162
SNPshot	rs122461162
SNPdbe	rs122461162
MSV3d	rs122461162
GWAS Ctlg	rs122461162

Max Magnitude

0

OMIM	300231
Desc
Variant	0002
Related	also

ClinVar
Risk	rs122461162(T;T)
Alt	rs122461162(T;T)
Reference	Rs122461162(C;C)
Significance	Pathogenic
Disease	Christianson syndrome
Variation	info
Gene	SLC9A6
CLNDBN	Christianson syndrome
Reversed	0
HGVS	NC_000023.10:g.135106524C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000012232.15,