rs397508201

Orientation

plus

Stabilized

plus

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

Make rs397508201(G;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117559462

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508201
dbSNP (classic)	rs397508201
ClinGen	rs397508201
ebi	rs397508201
HLI	rs397508201
Exac	rs397508201
Gnomad	rs397508201
Varsome	rs397508201
LitVar	rs397508201
Map	rs397508201
PheGenI	rs397508201
Biobank	rs397508201
1000 genomes	rs397508201
hgdp	rs397508201
ensembl	rs397508201
geneview	rs397508201
scholar	rs397508201
google	rs397508201
pharmgkb	rs397508201
gwascentral	rs397508201
openSNP	rs397508201
23andMe	rs397508201
SNPshot	rs397508201
SNPdbe	rs397508201
MSV3d	rs397508201
GWAS Ctlg	rs397508201

Max Magnitude

3

ClinVar
Risk	rs397508201(G;G)
Alt	rs397508201(G;G)
Reference	Rs397508201(A;A)
Significance	Pathogenic
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117199516A>G
CLNSRC	CFTR2
CLNACC	RCV000046291.4,