rs869025669

Orientation

minus

Stabilized

minus

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

Make rs869025669(C;C)

Make rs869025669(C;T)

Reference

GRCh38.p2 38.2/147

Chromosome

8

Position

38427970

Gene

FGFR1

is a	snp
is	mentioned by
dbSNP	rs869025669
dbSNP (classic)	rs869025669
ClinGen	rs869025669
ebi	rs869025669
HLI	rs869025669
Exac	rs869025669
Gnomad	rs869025669
Varsome	rs869025669
LitVar	rs869025669
Map	rs869025669
PheGenI	rs869025669
Biobank	rs869025669
1000 genomes	rs869025669
hgdp	rs869025669
ensembl	rs869025669
geneview	rs869025669
scholar	rs869025669
google	rs869025669
pharmgkb	rs869025669
gwascentral	rs869025669
openSNP	rs869025669
23andMe	rs869025669
SNPshot	rs869025669
SNPdbe	rs869025669
MSV3d	rs869025669
GWAS Ctlg	rs869025669

Max Magnitude

0

ClinVar
Risk	rs869025669(C;C)
Alt	rs869025669(C;C)
Reference	Rs869025669(T;T)
Significance	Pathogenic
Disease	Hartsfield syndrome
Variation	info
Gene	FGFR1
CLNDBN	Hartsfield syndrome
Reversed	1
HGVS	NC_000008.10:g.38285488A>G
CLNSRC
CLNACC	RCV000208879.1,