rs397508808

Orientation

plus

Stabilized

plus

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

Make rs397508808(C;T)

Make rs397508808(T;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117536672

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508808
dbSNP (classic)	rs397508808
ClinGen	rs397508808
ebi	rs397508808
HLI	rs397508808
Exac	rs397508808
Gnomad	rs397508808
Varsome	rs397508808
LitVar	rs397508808
Map	rs397508808
PheGenI	rs397508808
Biobank	rs397508808
1000 genomes	rs397508808
hgdp	rs397508808
ensembl	rs397508808
geneview	rs397508808
scholar	rs397508808
google	rs397508808
pharmgkb	rs397508808
gwascentral	rs397508808
openSNP	rs397508808
23andMe	rs397508808
SNPshot	rs397508808
SNPdbe	rs397508808
MSV3d	rs397508808
GWAS Ctlg	rs397508808

Max Magnitude

0

ClinVar
Risk	rs397508808(T;T)
Alt	rs397508808(T;T)
Reference	Rs397508808(C;C)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117176726C>T
CLNSRC	ClinVar
CLNACC	RCV000047274.2,