rs397508346

Orientation

plus

Stabilized

plus

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

Make rs397508346(T;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117592325

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508346
dbSNP (classic)	rs397508346
ClinGen	rs397508346
ebi	rs397508346
HLI	rs397508346
Exac	rs397508346
Gnomad	rs397508346
Varsome	rs397508346
LitVar	rs397508346
Map	rs397508346
PheGenI	rs397508346
Biobank	rs397508346
1000 genomes	rs397508346
hgdp	rs397508346
ensembl	rs397508346
geneview	rs397508346
scholar	rs397508346
google	rs397508346
pharmgkb	rs397508346
gwascentral	rs397508346
openSNP	rs397508346
23andMe	rs397508346
SNPshot	rs397508346
SNPdbe	rs397508346
MSV3d	rs397508346
GWAS Ctlg	rs397508346

Max Magnitude

3

ClinVar
Risk	rs397508346(T;T)
Alt	rs397508346(T;T)
Reference	Rs397508346(C;C)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117232379C>T
CLNSRC	ClinVar
CLNACC	RCV000046544.2,