rs397508268

Orientation

plus

Stabilized

plus

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

Make rs397508268(-;C)

Make rs397508268(C;C)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117590354

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508268
dbSNP (classic)	rs397508268
ClinGen	rs397508268
ebi	rs397508268
HLI	rs397508268
Exac	rs397508268
Gnomad	rs397508268
Varsome	rs397508268
LitVar	rs397508268
Map	rs397508268
PheGenI	rs397508268
Biobank	rs397508268
1000 genomes	rs397508268
hgdp	rs397508268
ensembl	rs397508268
geneview	rs397508268
scholar	rs397508268
google	rs397508268
pharmgkb	rs397508268
gwascentral	rs397508268
openSNP	rs397508268
23andMe	rs397508268
SNPshot	rs397508268
SNPdbe	rs397508268
MSV3d	rs397508268
GWAS Ctlg	rs397508268

Max Magnitude

0

ClinVar
Risk	rs397508268(C;C)
Alt	rs397508268(C;C)
Reference	Rs397508268(-;-)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117230409dupC
CLNSRC	ClinVar
CLNACC	RCV000046419.2,