rs397508274

Orientation

plus

Stabilized

plus

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

Make rs397508274(-;-)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117590376

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508274
dbSNP (classic)	rs397508274
ClinGen	rs397508274
ebi	rs397508274
HLI	rs397508274
Exac	rs397508274
Gnomad	rs397508274
Varsome	rs397508274
LitVar	rs397508274
Map	rs397508274
PheGenI	rs397508274
Biobank	rs397508274
1000 genomes	rs397508274
hgdp	rs397508274
ensembl	rs397508274
geneview	rs397508274
scholar	rs397508274
google	rs397508274
pharmgkb	rs397508274
gwascentral	rs397508274
openSNP	rs397508274
23andMe	rs397508274
SNPshot	rs397508274
SNPdbe	rs397508274
MSV3d	rs397508274
GWAS Ctlg	rs397508274

Max Magnitude

3

ClinVar
Risk	rs397508274(-;-)
Alt	rs397508274(-;-)
Reference	Rs397508274(T;T)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117230430delT
CLNSRC	ClinVar
CLNACC	RCV000046431.2,