rs797044906

Orientation

minus

Stabilized

minus

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

Make rs797044906(G;T)

Make rs797044906(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

215404591

Gene

FN1

is a	snp
is	mentioned by
dbSNP	rs797044906
dbSNP (classic)	rs797044906
ClinGen	rs797044906
ebi	rs797044906
HLI	rs797044906
Exac	rs797044906
Gnomad	rs797044906
Varsome	rs797044906
LitVar	rs797044906
Map	rs797044906
PheGenI	rs797044906
Biobank	rs797044906
1000 genomes	rs797044906
hgdp	rs797044906
ensembl	rs797044906
geneview	rs797044906
scholar	rs797044906
google	rs797044906
pharmgkb	rs797044906
gwascentral	rs797044906
openSNP	rs797044906
23andMe	rs797044906
SNPshot	rs797044906
SNPdbe	rs797044906
MSV3d	rs797044906
GWAS Ctlg	rs797044906

Max Magnitude

0

ClinVar
Risk	rs797044906(T;T)
Alt	rs797044906(T;T)
Reference	Rs797044906(G;G)
Significance	Pathogenic
Disease	Inborn genetic diseases
Variation	info
Gene	FN1
CLNDBN	Inborn genetic diseases
Reversed	1
HGVS	NC_000002.11:g.216269314C>A
CLNSRC
CLNACC	RCV000190733.1,