rs121908809

Orientation

plus

Stabilized

plus

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

Make rs121908809(-;-)

Make rs121908809(-;A)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117592143

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs121908809
dbSNP (classic)	rs121908809
ClinGen	rs121908809
ebi	rs121908809
HLI	rs121908809
Exac	rs121908809
Gnomad	rs121908809
Varsome	rs121908809
LitVar	rs121908809
Map	rs121908809
PheGenI	rs121908809
Biobank	rs121908809
1000 genomes	rs121908809
hgdp	rs121908809
ensembl	rs121908809
geneview	rs121908809
scholar	rs121908809
google	rs121908809
pharmgkb	rs121908809
gwascentral	rs121908809
openSNP	rs121908809
23andMe	rs121908809
SNPshot	rs121908809
SNPdbe	rs121908809
MSV3d	rs121908809
GWAS Ctlg	rs121908809

Max Magnitude

0

ClinVar
Risk	rs121908809(-;-)
Alt	rs121908809(-;-)
Reference	Rs121908809(A;A)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117232197delA
CLNSRC	ClinVar
CLNACC	RCV000046512.2,