rs797044911

Orientation

plus

Stabilized

plus

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

Make rs797044911(C;T)

Make rs797044911(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

19

Position

13025354

Gene

NFIX

is a	snp
is	mentioned by
dbSNP	rs797044911
dbSNP (classic)	rs797044911
ClinGen	rs797044911
ebi	rs797044911
HLI	rs797044911
Exac	rs797044911
Gnomad	rs797044911
Varsome	rs797044911
LitVar	rs797044911
Map	rs797044911
PheGenI	rs797044911
Biobank	rs797044911
1000 genomes	rs797044911
hgdp	rs797044911
ensembl	rs797044911
geneview	rs797044911
scholar	rs797044911
google	rs797044911
pharmgkb	rs797044911
gwascentral	rs797044911
openSNP	rs797044911
23andMe	rs797044911
SNPshot	rs797044911
SNPdbe	rs797044911
MSV3d	rs797044911
GWAS Ctlg	rs797044911

Max Magnitude

0

ClinVar
Risk	rs797044911(T;T)
Alt	rs797044911(T;T)
Reference	Rs797044911(C;C)
Significance	Pathogenic
Disease	Inborn genetic diseases
Variation	info
Gene	NFIX
CLNDBN	Inborn genetic diseases
Reversed	0
HGVS	NC_000019.9:g.13136168C>T
CLNSRC
CLNACC	RCV000190740.1,