rs121908775

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;CA)	3	carrier of a cystic fibrosis allele
(CA;CA)	0	common in clinvar

Make rs121908775(-;-)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117559548

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs121908775
dbSNP (classic)	rs121908775
ClinGen	rs121908775
ebi	rs121908775
HLI	rs121908775
Exac	rs121908775
Gnomad	rs121908775
Varsome	rs121908775
LitVar	rs121908775
Map	rs121908775
PheGenI	rs121908775
Biobank	rs121908775
1000 genomes	rs121908775
hgdp	rs121908775
ensembl	rs121908775
geneview	rs121908775
scholar	rs121908775
google	rs121908775
pharmgkb	rs121908775
gwascentral	rs121908775
openSNP	rs121908775
23andMe	rs121908775
SNPshot	rs121908775
SNPdbe	rs121908775
MSV3d	rs121908775
GWAS Ctlg	rs121908775

Max Magnitude

3

OMIM	602421
Desc
Variant	0115
Related	also

ClinVar
Risk	rs121908775(-;-)
Alt	rs121908775(-;-)
Reference	Rs121908775(CA;CA)
Significance	Pathogenic
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117199602_117199603delCA
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007640.3,