rs397508672

Orientation

plus

Stabilized

plus

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

Make rs397508672(-;-)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117531034

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508672
dbSNP (classic)	rs397508672
ClinGen	rs397508672
ebi	rs397508672
HLI	rs397508672
Exac	rs397508672
Gnomad	rs397508672
Varsome	rs397508672
LitVar	rs397508672
Map	rs397508672
PheGenI	rs397508672
Biobank	rs397508672
1000 genomes	rs397508672
hgdp	rs397508672
ensembl	rs397508672
geneview	rs397508672
scholar	rs397508672
google	rs397508672
pharmgkb	rs397508672
gwascentral	rs397508672
openSNP	rs397508672
23andMe	rs397508672
SNPshot	rs397508672
SNPdbe	rs397508672
MSV3d	rs397508672
GWAS Ctlg	rs397508672

Max Magnitude

3

ClinVar
Risk	rs397508672(-;-)
Alt	rs397508672(-;-)
Reference	Rs397508672(C;C)
Significance	Pathogenic
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117171088delC
CLNSRC	CFTR2
CLNACC	RCV000047072.3,