rs397508371

Orientation

plus

Stabilized

plus

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

Make rs397508371(A;A)

Make rs397508371(A;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117509105

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508371
dbSNP (classic)	rs397508371
ClinGen	rs397508371
ebi	rs397508371
HLI	rs397508371
Exac	rs397508371
Gnomad	rs397508371
Varsome	rs397508371
LitVar	rs397508371
Map	rs397508371
PheGenI	rs397508371
Biobank	rs397508371
1000 genomes	rs397508371
hgdp	rs397508371
ensembl	rs397508371
geneview	rs397508371
scholar	rs397508371
google	rs397508371
pharmgkb	rs397508371
gwascentral	rs397508371
openSNP	rs397508371
23andMe	rs397508371
SNPshot	rs397508371
SNPdbe	rs397508371
MSV3d	rs397508371
GWAS Ctlg	rs397508371

Max Magnitude

0

ClinVar
Risk	rs397508371(A;A)
Alt	rs397508371(A;A)
Reference	Rs397508371(G;G)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117149159G>A
CLNSRC	ClinVar
CLNACC	RCV000046584.2,