rs587779381

Orientation

plus

Stabilized

plus

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

Make rs587779381(C;G)

Make rs587779381(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

19

Position

13073924

Gene

NFIX

is a	snp
is	mentioned by
dbSNP	rs587779381
dbSNP (classic)	rs587779381
ClinGen	rs587779381
ebi	rs587779381
HLI	rs587779381
Exac	rs587779381
Gnomad	rs587779381
Varsome	rs587779381
LitVar	rs587779381
Map	rs587779381
PheGenI	rs587779381
Biobank	rs587779381
1000 genomes	rs587779381
hgdp	rs587779381
ensembl	rs587779381
geneview	rs587779381
scholar	rs587779381
google	rs587779381
pharmgkb	rs587779381
gwascentral	rs587779381
openSNP	rs587779381
23andMe	rs587779381
SNPshot	rs587779381
SNPdbe	rs587779381
MSV3d	rs587779381
GWAS Ctlg	rs587779381

Max Magnitude

0

ClinVar
Risk	rs587779381(G;G)
Alt	rs587779381(G;G)
Reference	Rs587779381(C;C)
Significance	Pathogenic
Disease	Sotos syndrome 2
Variation	info
Gene	NFIX
CLNDBN	Sotos syndrome 2
Reversed	0
HGVS	NC_000019.9:g.13184738C>G
CLNSRC
CLNACC	RCV000077780.1,