rs397508662

Orientation

plus

Stabilized

plus

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

Make rs397508662(-;-)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117664760

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508662
dbSNP (classic)	rs397508662
ClinGen	rs397508662
ebi	rs397508662
HLI	rs397508662
Exac	rs397508662
Gnomad	rs397508662
Varsome	rs397508662
LitVar	rs397508662
Map	rs397508662
PheGenI	rs397508662
Biobank	rs397508662
1000 genomes	rs397508662
hgdp	rs397508662
ensembl	rs397508662
geneview	rs397508662
scholar	rs397508662
google	rs397508662
pharmgkb	rs397508662
gwascentral	rs397508662
openSNP	rs397508662
23andMe	rs397508662
SNPshot	rs397508662
SNPdbe	rs397508662
MSV3d	rs397508662
GWAS Ctlg	rs397508662

Max Magnitude

3

ClinVar
Risk	rs397508662(-;-)
Alt	rs397508662(-;-)
Reference	Rs397508662(CCTAAGC;CCTAAGC)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117304814_117304820delCTAAGCC
CLNSRC	ClinVar
CLNACC	RCV000047059.2,