rs397508549

Orientation

plus

Stabilized

plus

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

Make rs397508549(A;T)

Make rs397508549(T;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117614627

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508549
dbSNP (classic)	rs397508549
ClinGen	rs397508549
ebi	rs397508549
HLI	rs397508549
Exac	rs397508549
Gnomad	rs397508549
Varsome	rs397508549
LitVar	rs397508549
Map	rs397508549
PheGenI	rs397508549
Biobank	rs397508549
1000 genomes	rs397508549
hgdp	rs397508549
ensembl	rs397508549
geneview	rs397508549
scholar	rs397508549
google	rs397508549
pharmgkb	rs397508549
gwascentral	rs397508549
openSNP	rs397508549
23andMe	rs397508549
SNPshot	rs397508549
SNPdbe	rs397508549
MSV3d	rs397508549
GWAS Ctlg	rs397508549

Max Magnitude

0

ClinVar
Risk	rs397508549(G;G) rs397508549(T;T)
Alt	rs397508549(G;G) rs397508549(T;T)
Reference	Rs397508549(A;A)
Significance	Untested
Disease	not specified Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	not specified Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117254681A>G; NC_000007.13:g.117254681A>T
CLNSRC	ClinVar
CLNACC	RCV000301584.1, RCV000046877.2,