rs730882054

Orientation

plus

Stabilized

plus

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

Make rs730882054(-;-)

Make rs730882054(-;CGGCGGCGCGG)

Make rs730882054(CGGCGGCGCGG;CGGCGGCGCGG)

Reference

GRCh38.p2 38.2/144

Chromosome

6

Position

1611579

Gene

FOXC1

is a	snp
is	mentioned by
dbSNP	rs730882054
dbSNP (classic)	rs730882054
ClinGen	rs730882054
ebi	rs730882054
HLI	rs730882054
Exac	rs730882054
Gnomad	rs730882054
Varsome	rs730882054
LitVar	rs730882054
Map	rs730882054
PheGenI	rs730882054
Biobank	rs730882054
1000 genomes	rs730882054
hgdp	rs730882054
ensembl	rs730882054
geneview	rs730882054
scholar	rs730882054
google	rs730882054
pharmgkb	rs730882054
gwascentral	rs730882054
openSNP	rs730882054
23andMe	rs730882054
SNPshot	rs730882054
SNPdbe	rs730882054
MSV3d	rs730882054
GWAS Ctlg	rs730882054

Max Magnitude

0

ClinVar
Risk	rs730882054(-;-)
Alt	rs730882054(-;-)
Reference	Rs730882054(GCGGCGGCGGC;GCGGCGGCGGC)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FOXC1
CLNDBN	not provided
Reversed	0
HGVS	NC_000006.11:g.1611814_1611824delCGGCGGCGCGG
CLNSRC
CLNACC	RCV000162085.1,