rs387906380

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	0	common in clinvar
(-;A)	3	cystic fibrosis carrier

Make rs387906380(A;A)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117536664

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs387906380
dbSNP (classic)	rs387906380
ClinGen	rs387906380
ebi	rs387906380
HLI	rs387906380
Exac	rs387906380
Gnomad	rs387906380
Varsome	rs387906380
LitVar	rs387906380
Map	rs387906380
PheGenI	rs387906380
Biobank	rs387906380
1000 genomes	rs387906380
hgdp	rs387906380
ensembl	rs387906380
geneview	rs387906380
scholar	rs387906380
google	rs387906380
pharmgkb	rs387906380
gwascentral	rs387906380
openSNP	rs387906380
23andMe	rs387906380
SNPshot	rs387906380
SNPdbe	rs387906380
MSV3d	rs387906380
GWAS Ctlg	rs387906380

Merged from

Rs397508803

Max Magnitude

3

ClinVar
Risk	rs387906380(A;A)
Alt	rs387906380(A;A)
Reference	Rs387906380(-;-)
Significance	Pathogenic
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117176718dupA
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007658.4,