rs397508150

Orientation

plus

Stabilized

plus

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

Make rs397508150(A;A)

Make rs397508150(A;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117540298

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508150
dbSNP (classic)	rs397508150
ClinGen	rs397508150
ebi	rs397508150
HLI	rs397508150
Exac	rs397508150
Gnomad	rs397508150
Varsome	rs397508150
LitVar	rs397508150
Map	rs397508150
PheGenI	rs397508150
Biobank	rs397508150
1000 genomes	rs397508150
hgdp	rs397508150
ensembl	rs397508150
geneview	rs397508150
scholar	rs397508150
google	rs397508150
pharmgkb	rs397508150
gwascentral	rs397508150
openSNP	rs397508150
23andMe	rs397508150
SNPshot	rs397508150
SNPdbe	rs397508150
MSV3d	rs397508150
GWAS Ctlg	rs397508150

Max Magnitude

0

ClinVar
Risk	rs397508150(A;A)
Alt	rs397508150(A;A)
Reference	Rs397508150(G;G)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117180352G>A
CLNSRC	ClinVar
CLNACC	RCV000046218.2,