rs121908754

Orientation

plus

Stabilized

plus

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

Make rs121908754(A;A)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117559643

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs121908754
dbSNP (classic)	rs121908754
ClinGen	rs121908754
ebi	rs121908754
HLI	rs121908754
Exac	rs121908754
Gnomad	rs121908754
Varsome	rs121908754
LitVar	rs121908754
Map	rs121908754
PheGenI	rs121908754
Biobank	rs121908754
1000 genomes	rs121908754
hgdp	rs121908754
ensembl	rs121908754
geneview	rs121908754
scholar	rs121908754
google	rs121908754
pharmgkb	rs121908754
gwascentral	rs121908754
openSNP	rs121908754
23andMe	rs121908754
SNPshot	rs121908754
SNPdbe	rs121908754
MSV3d	rs121908754
GWAS Ctlg	rs121908754

Merged from

Rs121909014

Max Magnitude

3

OMIM	602421
Desc
Variant	0047
Related	also

ClinVar
Risk	rs121908754(A;A)
Alt	rs121908754(A;A)
Reference	Rs121908754(C;C)
Significance	Pathogenic
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117199697C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007571.3,