rs876661328

Orientation

minus

Stabilized

minus

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

Make rs876661328(A;A)

Make rs876661328(A;C)

Reference

GRCh38.p2 38.2/147

Chromosome

10

Position

101774752

Gene

FGF8

is a	snp
is	mentioned by
dbSNP	rs876661328
dbSNP (classic)	rs876661328
ClinGen	rs876661328
ebi	rs876661328
HLI	rs876661328
Exac	rs876661328
Gnomad	rs876661328
Varsome	rs876661328
LitVar	rs876661328
Map	rs876661328
PheGenI	rs876661328
Biobank	rs876661328
1000 genomes	rs876661328
hgdp	rs876661328
ensembl	rs876661328
geneview	rs876661328
scholar	rs876661328
google	rs876661328
pharmgkb	rs876661328
gwascentral	rs876661328
openSNP	rs876661328
23andMe	rs876661328
SNPshot	rs876661328
SNPdbe	rs876661328
MSV3d	rs876661328
GWAS Ctlg	rs876661328

Max Magnitude

0

ClinVar
Risk	rs876661328(A;A)
Alt	rs876661328(A;A)
Reference	Rs876661328(C;C)
Significance	Probable-Pathogenic
Disease	Semilobar holoprosencephaly
Variation	info
Gene	FGF8
CLNDBN	Semilobar holoprosencephaly
Reversed	1
HGVS	NC_000010.10:g.103534509G>T
CLNSRC
CLNACC	RCV000223804.1,