rs797045738

Orientation

plus

Stabilized

plus

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

Make rs797045738(-;-)

Make rs797045738(-;AA)

Reference

GRCh38.p2 38.2/147

Chromosome

19

Position

13078627

Gene

NFIX

is a	snp
is	mentioned by
dbSNP	rs797045738
dbSNP (classic)	rs797045738
ClinGen	rs797045738
ebi	rs797045738
HLI	rs797045738
Exac	rs797045738
Gnomad	rs797045738
Varsome	rs797045738
LitVar	rs797045738
Map	rs797045738
PheGenI	rs797045738
Biobank	rs797045738
1000 genomes	rs797045738
hgdp	rs797045738
ensembl	rs797045738
geneview	rs797045738
scholar	rs797045738
google	rs797045738
pharmgkb	rs797045738
gwascentral	rs797045738
openSNP	rs797045738
23andMe	rs797045738
SNPshot	rs797045738
SNPdbe	rs797045738
MSV3d	rs797045738
GWAS Ctlg	rs797045738

Max Magnitude

0

ClinVar
Risk	rs797045738(-;-)
Alt	rs797045738(-;-)
Reference	Rs797045738(AA;AA)
Significance	Pathogenic
Disease	Marshall-Smith syndrome
Variation	info
Gene	NFIX
CLNDBN	Marshall-Smith syndrome
Reversed	0
HGVS	NC_000019.9:g.13189441_13189442delAA
CLNSRC
CLNACC	RCV000194821.1,