rs397508270

Orientation

plus

Stabilized

plus

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

Make rs397508270(A;G)

Make rs397508270(G;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117590367

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508270
dbSNP (classic)	rs397508270
ClinGen	rs397508270
ebi	rs397508270
HLI	rs397508270
Exac	rs397508270
Gnomad	rs397508270
Varsome	rs397508270
LitVar	rs397508270
Map	rs397508270
PheGenI	rs397508270
Biobank	rs397508270
1000 genomes	rs397508270
hgdp	rs397508270
ensembl	rs397508270
geneview	rs397508270
scholar	rs397508270
google	rs397508270
pharmgkb	rs397508270
gwascentral	rs397508270
openSNP	rs397508270
23andMe	rs397508270
SNPshot	rs397508270
SNPdbe	rs397508270
MSV3d	rs397508270
GWAS Ctlg	rs397508270

Max Magnitude

0

ClinVar
Risk	rs397508270(G;G)
Alt	rs397508270(G;G)
Reference	Rs397508270(A;A)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117230421A>G
CLNSRC	ClinVar
CLNACC	RCV000046426.2,