rs869025672

Orientation

minus

Stabilized

minus

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

Make rs869025672(G;G)

Make rs869025672(G;T)

Reference

GRCh38.p2 38.2/147

Chromosome

8

Position

38414872

Gene

FGFR1

is a	snp
is	mentioned by
dbSNP	rs869025672
dbSNP (classic)	rs869025672
ClinGen	rs869025672
ebi	rs869025672
HLI	rs869025672
Exac	rs869025672
Gnomad	rs869025672
Varsome	rs869025672
LitVar	rs869025672
Map	rs869025672
PheGenI	rs869025672
Biobank	rs869025672
1000 genomes	rs869025672
hgdp	rs869025672
ensembl	rs869025672
geneview	rs869025672
scholar	rs869025672
google	rs869025672
pharmgkb	rs869025672
gwascentral	rs869025672
openSNP	rs869025672
23andMe	rs869025672
SNPshot	rs869025672
SNPdbe	rs869025672
MSV3d	rs869025672
GWAS Ctlg	rs869025672

Max Magnitude

0

ClinVar
Risk	rs869025672(G;G)
Alt	rs869025672(G;G)
Reference	Rs869025672(T;T)
Significance	Pathogenic
Disease	Hartsfield syndrome
Variation	info
Gene	FGFR1
CLNDBN	Hartsfield syndrome
Reversed	1
HGVS	NC_000008.10:g.38272390A>C
CLNSRC
CLNACC	RCV000208876.1,