rs876661332

Orientation

minus

Stabilized

minus

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

Make rs876661332(G;T)

Make rs876661332(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

8

Position

38417968

Gene

FGFR1

is a	snp
is	mentioned by
dbSNP	rs876661332
dbSNP (classic)	rs876661332
ClinGen	rs876661332
ebi	rs876661332
HLI	rs876661332
Exac	rs876661332
Gnomad	rs876661332
Varsome	rs876661332
LitVar	rs876661332
Map	rs876661332
PheGenI	rs876661332
Biobank	rs876661332
1000 genomes	rs876661332
hgdp	rs876661332
ensembl	rs876661332
geneview	rs876661332
scholar	rs876661332
google	rs876661332
pharmgkb	rs876661332
gwascentral	rs876661332
openSNP	rs876661332
23andMe	rs876661332
SNPshot	rs876661332
SNPdbe	rs876661332
MSV3d	rs876661332
GWAS Ctlg	rs876661332

Max Magnitude

0

ClinVar
Risk	rs876661332(T;T)
Alt	rs876661332(T;T)
Reference	Rs876661332(G;G)
Significance	Probable-Pathogenic
Disease	Hartsfield syndrome
Variation	info
Gene	FGFR1
CLNDBN	Hartsfield syndrome
Reversed	1
HGVS	NC_000008.10:g.38275486C>A
CLNSRC
CLNACC	RCV000223739.1,