rs138918423

Orientation

plus

Stabilized

plus

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

Make rs138918423(C;T)

Make rs138918423(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

149487059

Gene

IDS

is a	snp
is	mentioned by
dbSNP	rs138918423
dbSNP (classic)	rs138918423
ClinGen	rs138918423
ebi	rs138918423
HLI	rs138918423
Exac	rs138918423
Gnomad	rs138918423
Varsome	rs138918423
LitVar	rs138918423
Map	rs138918423
PheGenI	rs138918423
Biobank	rs138918423
1000 genomes	rs138918423
hgdp	rs138918423
ensembl	rs138918423
geneview	rs138918423
scholar	rs138918423
google	rs138918423
pharmgkb	rs138918423
gwascentral	rs138918423
openSNP	rs138918423
23andMe	rs138918423
SNPshot	rs138918423
SNPdbe	rs138918423
MSV3d	rs138918423
GWAS Ctlg	rs138918423

Max Magnitude

0

ClinVar
Risk	rs138918423(T;T)
Alt	rs138918423(T;T)
Reference	Rs138918423(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	IDS
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.148568590C>T
CLNSRC
CLNACC	RCV000478817.1,