rs121909337

Orientation

plus

Stabilized

plus

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

Make rs121909337(C;C)

Make rs121909337(C;T)

Reference

GRCh38 38.1/141

Chromosome

16

Position

86513083

Gene

FOXF1

is a	snp
is	mentioned by
dbSNP	rs121909337
dbSNP (classic)	rs121909337
ClinGen	rs121909337
ebi	rs121909337
HLI	rs121909337
Exac	rs121909337
Gnomad	rs121909337
Varsome	rs121909337
LitVar	rs121909337
Map	rs121909337
PheGenI	rs121909337
Biobank	rs121909337
1000 genomes	rs121909337
hgdp	rs121909337
ensembl	rs121909337
geneview	rs121909337
scholar	rs121909337
google	rs121909337
pharmgkb	rs121909337
gwascentral	rs121909337
openSNP	rs121909337
23andMe	rs121909337
SNPshot	rs121909337
SNPdbe	rs121909337
MSV3d	rs121909337
GWAS Ctlg	rs121909337

Max Magnitude

0

OMIM	601089
Desc
Variant	0002
Related	also

ClinVar
Risk	rs121909337(C;C)
Alt	rs121909337(C;C)
Reference	Rs121909337(T;T)
Significance	Pathogenic
Disease	Alveolar capillary dysplasia with misalignment of pulmonary veins
Variation	info
Gene	FOXF1
CLNDBN	Alveolar capillary dysplasia with misalignment of pulmonary veins
Reversed	0
HGVS	NC_000016.9:g.86546689T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008984.3,