rs397508578

Orientation

plus

Stabilized

plus

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

Make rs397508578(A;T)

Make rs397508578(T;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117627582

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508578
dbSNP (classic)	rs397508578
ClinGen	rs397508578
ebi	rs397508578
HLI	rs397508578
Exac	rs397508578
Gnomad	rs397508578
Varsome	rs397508578
LitVar	rs397508578
Map	rs397508578
PheGenI	rs397508578
Biobank	rs397508578
1000 genomes	rs397508578
hgdp	rs397508578
ensembl	rs397508578
geneview	rs397508578
scholar	rs397508578
google	rs397508578
pharmgkb	rs397508578
gwascentral	rs397508578
openSNP	rs397508578
23andMe	rs397508578
SNPshot	rs397508578
SNPdbe	rs397508578
MSV3d	rs397508578
GWAS Ctlg	rs397508578

Max Magnitude

0

ClinVar
Risk	rs397508578(T;T)
Alt	rs397508578(T;T)
Reference	Rs397508578(A;A)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117267636A>T
CLNSRC	ClinVar
CLNACC	RCV000046921.2,