rs397508230

Orientation

plus

Stabilized

plus

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

Make rs397508230(A;A)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117559656

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508230
dbSNP (classic)	rs397508230
ClinGen	rs397508230
ebi	rs397508230
HLI	rs397508230
Exac	rs397508230
Gnomad	rs397508230
Varsome	rs397508230
LitVar	rs397508230
Map	rs397508230
PheGenI	rs397508230
Biobank	rs397508230
1000 genomes	rs397508230
hgdp	rs397508230
ensembl	rs397508230
geneview	rs397508230
scholar	rs397508230
google	rs397508230
pharmgkb	rs397508230
gwascentral	rs397508230
openSNP	rs397508230
23andMe	rs397508230
SNPshot	rs397508230
SNPdbe	rs397508230
MSV3d	rs397508230
GWAS Ctlg	rs397508230

Max Magnitude

3

ClinVar
Risk	rs397508230(A;A) rs397508230(T;T)
Alt	rs397508230(A;A) rs397508230(T;T)
Reference	Rs397508230(G;G)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117199710G>A; NC_000007.13:g.117199710G>T
CLNSRC	ClinVar
CLNACC	RCV000046346.2, RCV000046347.2,