rs397508267

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar
(A;C)	3	carrier of a cystic fibrosis allele

Make rs397508267(C;C)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117590353

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508267
dbSNP (classic)	rs397508267
ClinGen	rs397508267
ebi	rs397508267
HLI	rs397508267
Exac	rs397508267
Gnomad	rs397508267
Varsome	rs397508267
LitVar	rs397508267
Map	rs397508267
PheGenI	rs397508267
Biobank	rs397508267
1000 genomes	rs397508267
hgdp	rs397508267
ensembl	rs397508267
geneview	rs397508267
scholar	rs397508267
google	rs397508267
pharmgkb	rs397508267
gwascentral	rs397508267
openSNP	rs397508267
23andMe	rs397508267
SNPshot	rs397508267
SNPdbe	rs397508267
MSV3d	rs397508267
GWAS Ctlg	rs397508267

Max Magnitude

3

ClinVar
Risk	rs397508267(C;C)
Alt	rs397508267(C;C)
Reference	Rs397508267(A;A)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117230407A>C
CLNSRC	ClinVar
CLNACC	RCV000046418.2,