rs397508528

Orientation

plus

Stabilized

plus

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

Make rs397508528(A;A)

Make rs397508528(A;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117530952

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508528
dbSNP (classic)	rs397508528
ClinGen	rs397508528
ebi	rs397508528
HLI	rs397508528
Exac	rs397508528
Gnomad	rs397508528
Varsome	rs397508528
LitVar	rs397508528
Map	rs397508528
PheGenI	rs397508528
Biobank	rs397508528
1000 genomes	rs397508528
hgdp	rs397508528
ensembl	rs397508528
geneview	rs397508528
scholar	rs397508528
google	rs397508528
pharmgkb	rs397508528
gwascentral	rs397508528
openSNP	rs397508528
23andMe	rs397508528
SNPshot	rs397508528
SNPdbe	rs397508528
MSV3d	rs397508528
GWAS Ctlg	rs397508528

Max Magnitude

0

ClinVar
Risk	rs397508528(A;A)
Alt	rs397508528(A;A)
Reference	Rs397508528(T;T)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117171006T>A
CLNSRC	ClinVar
CLNACC	RCV000046848.2,