rs121908773

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;AT)	3	cystic fibrosis carrier
(AT;AT)	0	common in clinvar

Make rs121908773(-;-)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117536609

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs121908773
dbSNP (classic)	rs121908773
ClinGen	rs121908773
ebi	rs121908773
HLI	rs121908773
Exac	rs121908773
Gnomad	rs121908773
Varsome	rs121908773
LitVar	rs121908773
Map	rs121908773
PheGenI	rs121908773
Biobank	rs121908773
1000 genomes	rs121908773
hgdp	rs121908773
ensembl	rs121908773
geneview	rs121908773
scholar	rs121908773
google	rs121908773
pharmgkb	rs121908773
gwascentral	rs121908773
openSNP	rs121908773
23andMe	rs121908773
SNPshot	rs121908773
SNPdbe	rs121908773
MSV3d	rs121908773
GWAS Ctlg	rs121908773

Max Magnitude

3

OMIM	602421
Desc
Variant	0101
Related	also

ClinVar
Risk	rs121908773(-;-)
Alt	rs121908773(-;-)
Reference	Rs121908773(AT;AT)
Significance	Pathogenic
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117176663_117176664delAT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007627.3,