rs398122874

Orientation

plus

Stabilized

plus

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

Make rs398122874(-;T)

Make rs398122874(T;T)

Reference

GRCh38 38.1/141

Chromosome

19

Position

13078651

Gene

NFIX

is a	snp
is	mentioned by
dbSNP	rs398122874
dbSNP (classic)	rs398122874
ClinGen	rs398122874
ebi	rs398122874
HLI	rs398122874
Exac	rs398122874
Gnomad	rs398122874
Varsome	rs398122874
LitVar	rs398122874
Map	rs398122874
PheGenI	rs398122874
Biobank	rs398122874
1000 genomes	rs398122874
hgdp	rs398122874
ensembl	rs398122874
geneview	rs398122874
scholar	rs398122874
google	rs398122874
pharmgkb	rs398122874
gwascentral	rs398122874
openSNP	rs398122874
23andMe	rs398122874
SNPshot	rs398122874
SNPdbe	rs398122874
MSV3d	rs398122874
GWAS Ctlg	rs398122874

Max Magnitude

0

ClinVar
Risk	rs398122874(T;T)
Alt	rs398122874(T;T)
Reference	Rs398122874(-;-)
Significance	Pathogenic
Disease	Marshall-Smith syndrome
Variation	info
Gene	NFIX
CLNDBN	Marshall-Smith syndrome
Reversed	0
HGVS	NC_000019.9:g.13189465dupT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000030642.25,