rs397508684

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	3	carrier of a cystic fibrosis allele

Make rs397508684(T;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117665466

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508684
dbSNP (classic)	rs397508684
ClinGen	rs397508684
ebi	rs397508684
HLI	rs397508684
Exac	rs397508684
Gnomad	rs397508684
Varsome	rs397508684
LitVar	rs397508684
Map	rs397508684
PheGenI	rs397508684
Biobank	rs397508684
1000 genomes	rs397508684
hgdp	rs397508684
ensembl	rs397508684
geneview	rs397508684
scholar	rs397508684
google	rs397508684
pharmgkb	rs397508684
gwascentral	rs397508684
openSNP	rs397508684
23andMe	rs397508684
SNPshot	rs397508684
SNPdbe	rs397508684
MSV3d	rs397508684
GWAS Ctlg	rs397508684

Max Magnitude

3

ClinVar
Risk	rs397508684(A;A) rs397508684(T;T)
Alt	rs397508684(A;A) rs397508684(T;T)
Reference	Rs397508684(C;C)
Significance	Pathogenic
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117305520C>T
CLNSRC	CFTR2
CLNACC	RCV000047087.3,