rs397508177

Orientation

plus

Stabilized

plus

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

Make rs397508177(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

7

Position

117542108

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508177
dbSNP (classic)	rs397508177
ClinGen	rs397508177
ebi	rs397508177
HLI	rs397508177
Exac	rs397508177
Gnomad	rs397508177
Varsome	rs397508177
LitVar	rs397508177
Map	rs397508177
PheGenI	rs397508177
Biobank	rs397508177
1000 genomes	rs397508177
hgdp	rs397508177
ensembl	rs397508177
geneview	rs397508177
scholar	rs397508177
google	rs397508177
pharmgkb	rs397508177
gwascentral	rs397508177
openSNP	rs397508177
23andMe	rs397508177
SNPshot	rs397508177
SNPdbe	rs397508177
MSV3d	rs397508177
GWAS Ctlg	rs397508177

Max Magnitude

3

ClinVar
Risk	rs397508177(A;A) rs397508177(C;C)
Alt	rs397508177(A;A) rs397508177(C;C)
Reference	Rs397508177(G;G)
Significance	Untested
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117182162G>A; NC_000007.13:g.117182162G>C
CLNSRC
CLNACC	RCV000046259.2, RCV000046260.2,