rs397508604

Orientation

plus

Stabilized

plus

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

Make rs397508604(G;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117642481

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508604
dbSNP (classic)	rs397508604
ClinGen	rs397508604
ebi	rs397508604
HLI	rs397508604
Exac	rs397508604
Gnomad	rs397508604
Varsome	rs397508604
LitVar	rs397508604
Map	rs397508604
PheGenI	rs397508604
Biobank	rs397508604
1000 genomes	rs397508604
hgdp	rs397508604
ensembl	rs397508604
geneview	rs397508604
scholar	rs397508604
google	rs397508604
pharmgkb	rs397508604
gwascentral	rs397508604
openSNP	rs397508604
23andMe	rs397508604
SNPshot	rs397508604
SNPdbe	rs397508604
MSV3d	rs397508604
GWAS Ctlg	rs397508604

Max Magnitude

3

ClinVar
Risk	rs397508604(G;G)
Alt	rs397508604(G;G)
Reference	Rs397508604(T;T)
Significance	Pathogenic
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117282535T>G
CLNSRC	CFTR2
CLNACC	RCV000046973.3,