rs397508258

Orientation

plus

Stabilized

plus

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

Make rs397508258(-;-)

Make rs397508258(-;A)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117587828

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508258
dbSNP (classic)	rs397508258
ClinGen	rs397508258
ebi	rs397508258
HLI	rs397508258
Exac	rs397508258
Gnomad	rs397508258
Varsome	rs397508258
LitVar	rs397508258
Map	rs397508258
PheGenI	rs397508258
Biobank	rs397508258
1000 genomes	rs397508258
hgdp	rs397508258
ensembl	rs397508258
geneview	rs397508258
scholar	rs397508258
google	rs397508258
pharmgkb	rs397508258
gwascentral	rs397508258
openSNP	rs397508258
23andMe	rs397508258
SNPshot	rs397508258
SNPdbe	rs397508258
MSV3d	rs397508258
GWAS Ctlg	rs397508258

Max Magnitude

0

ClinVar
Risk	rs397508258(-;-)
Alt	rs397508258(-;-)
Reference	Rs397508258(A;A)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117227882delA
CLNSRC	ClinVar
CLNACC	RCV000046402.2,