rs797044864

Orientation

plus

Stabilized

plus

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

Make rs797044864(A;A)

Make rs797044864(A;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

48478081

Gene

FTSJ1

is a	snp
is	mentioned by
dbSNP	rs797044864
dbSNP (classic)	rs797044864
ClinGen	rs797044864
ebi	rs797044864
HLI	rs797044864
Exac	rs797044864
Gnomad	rs797044864
Varsome	rs797044864
LitVar	rs797044864
Map	rs797044864
PheGenI	rs797044864
Biobank	rs797044864
1000 genomes	rs797044864
hgdp	rs797044864
ensembl	rs797044864
geneview	rs797044864
scholar	rs797044864
google	rs797044864
pharmgkb	rs797044864
gwascentral	rs797044864
openSNP	rs797044864
23andMe	rs797044864
SNPshot	rs797044864
SNPdbe	rs797044864
MSV3d	rs797044864
GWAS Ctlg	rs797044864

Max Magnitude

0

ClinVar
Risk	rs797044864(A;A)
Alt	rs797044864(A;A)
Reference	Rs797044864(T;T)
Significance	Pathogenic
Disease	Inborn genetic diseases
Variation	info
Gene	FTSJ1
CLNDBN	Inborn genetic diseases
Reversed	0
HGVS	NC_000023.10:g.48336469T>A
CLNSRC
CLNACC	RCV000190669.1,