rs397508410

Orientation

plus

Stabilized

plus

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

Make rs397508410(C;C)

Make rs397508410(C;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117602825

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508410
dbSNP (classic)	rs397508410
ClinGen	rs397508410
ebi	rs397508410
HLI	rs397508410
Exac	rs397508410
Gnomad	rs397508410
Varsome	rs397508410
LitVar	rs397508410
Map	rs397508410
PheGenI	rs397508410
Biobank	rs397508410
1000 genomes	rs397508410
hgdp	rs397508410
ensembl	rs397508410
geneview	rs397508410
scholar	rs397508410
google	rs397508410
pharmgkb	rs397508410
gwascentral	rs397508410
openSNP	rs397508410
23andMe	rs397508410
SNPshot	rs397508410
SNPdbe	rs397508410
MSV3d	rs397508410
GWAS Ctlg	rs397508410

Max Magnitude

0

ClinVar
Risk	rs397508410(C;C) rs397508410(T;T)
Alt	rs397508410(C;C) rs397508410(T;T)
Reference	Rs397508410(G;G)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117242879G>C; NC_000007.13:g.117242879G>T
CLNSRC	ClinVar
CLNACC	RCV000046636.2, RCV000046637.2,