rs397508815

Orientation

plus

Stabilized

plus

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

Make rs397508815(T;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117504287

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508815
dbSNP (classic)	rs397508815
ClinGen	rs397508815
ebi	rs397508815
HLI	rs397508815
Exac	rs397508815
Gnomad	rs397508815
Varsome	rs397508815
LitVar	rs397508815
Map	rs397508815
PheGenI	rs397508815
Biobank	rs397508815
1000 genomes	rs397508815
hgdp	rs397508815
ensembl	rs397508815
geneview	rs397508815
scholar	rs397508815
google	rs397508815
pharmgkb	rs397508815
gwascentral	rs397508815
openSNP	rs397508815
23andMe	rs397508815
SNPshot	rs397508815
SNPdbe	rs397508815
MSV3d	rs397508815
GWAS Ctlg	rs397508815

Max Magnitude

3

ClinVar
Risk	rs397508815(T;T)
Alt	rs397508815(T;T)
Reference	Rs397508815(C;C)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117144341C>T
CLNSRC	ClinVar
CLNACC	RCV000047281.2,