rs886039429

Orientation

plus

Stabilized

plus

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

Make rs886039429(C;T)

Make rs886039429(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

1

Position

61088482

Gene

NFIA

is a	snp
is	mentioned by
dbSNP	rs886039429
dbSNP (classic)	rs886039429
ClinGen	rs886039429
ebi	rs886039429
HLI	rs886039429
Exac	rs886039429
Gnomad	rs886039429
Varsome	rs886039429
LitVar	rs886039429
Map	rs886039429
PheGenI	rs886039429
Biobank	rs886039429
1000 genomes	rs886039429
hgdp	rs886039429
ensembl	rs886039429
geneview	rs886039429
scholar	rs886039429
google	rs886039429
pharmgkb	rs886039429
gwascentral	rs886039429
openSNP	rs886039429
23andMe	rs886039429
SNPshot	rs886039429
SNPdbe	rs886039429
MSV3d	rs886039429
GWAS Ctlg	rs886039429

Max Magnitude

0

ClinVar
Risk	rs886039429(T;T)
Alt	rs886039429(T;T)
Reference	Rs886039429(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	NFIA
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.61554154C>T
CLNSRC
CLNACC	RCV000254980.1,