rs387906362

Orientation

plus

Stabilized

plus

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

Make rs387906362(G;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117627774

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs387906362
dbSNP (classic)	rs387906362
ClinGen	rs387906362
ebi	rs387906362
HLI	rs387906362
Exac	rs387906362
Gnomad	rs387906362
Varsome	rs387906362
LitVar	rs387906362
Map	rs387906362
PheGenI	rs387906362
Biobank	rs387906362
1000 genomes	rs387906362
hgdp	rs387906362
ensembl	rs387906362
geneview	rs387906362
scholar	rs387906362
google	rs387906362
pharmgkb	rs387906362
gwascentral	rs387906362
openSNP	rs387906362
23andMe	rs387906362
SNPshot	rs387906362
SNPdbe	rs387906362
MSV3d	rs387906362
GWAS Ctlg	rs387906362

Max Magnitude

3

ClinVar
Risk	rs387906362(G;G)
Alt	rs387906362(G;G)
Reference	Rs387906362(A;A)
Significance	Pathogenic
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117267828A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007558.3,