rs397508441

Orientation

plus

Stabilized

plus

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

Make rs397508441(-;-)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117603699

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508441
dbSNP (classic)	rs397508441
ClinGen	rs397508441
ebi	rs397508441
HLI	rs397508441
Exac	rs397508441
Gnomad	rs397508441
Varsome	rs397508441
LitVar	rs397508441
Map	rs397508441
PheGenI	rs397508441
Biobank	rs397508441
1000 genomes	rs397508441
hgdp	rs397508441
ensembl	rs397508441
geneview	rs397508441
scholar	rs397508441
google	rs397508441
pharmgkb	rs397508441
gwascentral	rs397508441
openSNP	rs397508441
23andMe	rs397508441
SNPshot	rs397508441
SNPdbe	rs397508441
MSV3d	rs397508441
GWAS Ctlg	rs397508441

Max Magnitude

3

ClinVar
Risk	rs397508441(-;-)
Alt	rs397508441(-;-)
Reference	Rs397508441(T;T)
Significance	Pathogenic
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117243753delT
CLNSRC	CFTR2
CLNACC	RCV000046696.3,