rs397508281

Orientation

plus

Stabilized

plus

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

Make rs397508281(-;-)

Make rs397508281(-;AG)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117590386

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508281
dbSNP (classic)	rs397508281
ClinGen	rs397508281
ebi	rs397508281
HLI	rs397508281
Exac	rs397508281
Gnomad	rs397508281
Varsome	rs397508281
LitVar	rs397508281
Map	rs397508281
PheGenI	rs397508281
Biobank	rs397508281
1000 genomes	rs397508281
hgdp	rs397508281
ensembl	rs397508281
geneview	rs397508281
scholar	rs397508281
google	rs397508281
pharmgkb	rs397508281
gwascentral	rs397508281
openSNP	rs397508281
23andMe	rs397508281
SNPshot	rs397508281
SNPdbe	rs397508281
MSV3d	rs397508281
GWAS Ctlg	rs397508281

Max Magnitude

0

ClinVar
Risk	rs397508281(-;-)
Alt	rs397508281(-;-)
Reference	Rs397508281(AG;AG)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117230440_117230441delAG
CLNSRC	ClinVar
CLNACC	RCV000046439.2,