rs397508216

Orientation

plus

Stabilized

plus

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

Make rs397508216(A;A)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117559558

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508216
dbSNP (classic)	rs397508216
ClinGen	rs397508216
ebi	rs397508216
HLI	rs397508216
Exac	rs397508216
Gnomad	rs397508216
Varsome	rs397508216
LitVar	rs397508216
Map	rs397508216
PheGenI	rs397508216
Biobank	rs397508216
1000 genomes	rs397508216
hgdp	rs397508216
ensembl	rs397508216
geneview	rs397508216
scholar	rs397508216
google	rs397508216
pharmgkb	rs397508216
gwascentral	rs397508216
openSNP	rs397508216
23andMe	rs397508216
SNPshot	rs397508216
SNPdbe	rs397508216
MSV3d	rs397508216
GWAS Ctlg	rs397508216

Max Magnitude

3

ClinVar
Risk	rs397508216(A;A)
Alt	rs397508216(A;A)
Reference	Rs397508216(G;G)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117199612G>A
CLNSRC	ClinVar
CLNACC	RCV000046318.2,