rs397508356

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(CCTCGCAT;CCTCGCAT)	0	common in clinvar

Make rs397508356(-;-)

Make rs397508356(-;CCTCGCAT)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117592415

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508356
dbSNP (classic)	rs397508356
ClinGen	rs397508356
ebi	rs397508356
HLI	rs397508356
Exac	rs397508356
Gnomad	rs397508356
Varsome	rs397508356
LitVar	rs397508356
Map	rs397508356
PheGenI	rs397508356
Biobank	rs397508356
1000 genomes	rs397508356
hgdp	rs397508356
ensembl	rs397508356
geneview	rs397508356
scholar	rs397508356
google	rs397508356
pharmgkb	rs397508356
gwascentral	rs397508356
openSNP	rs397508356
23andMe	rs397508356
SNPshot	rs397508356
SNPdbe	rs397508356
MSV3d	rs397508356
GWAS Ctlg	rs397508356

Max Magnitude

0

ClinVar
Risk	rs397508356(-;-)
Alt	rs397508356(-;-)
Reference	Rs397508356(CCTCGCAT;CCTCGCAT)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117232469_117232476delCCTCGCAT
CLNSRC	ClinVar
CLNACC	RCV000046560.2,