rs397508628

Merged into

rs387906373

Orientation

plus

Stabilized

plus

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

Make rs397508628(-;-)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117652850

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508628
dbSNP (classic)	rs397508628
ClinGen	rs397508628
ebi	rs397508628
HLI	rs397508628
Exac	rs397508628
Gnomad	rs397508628
Varsome	rs397508628
LitVar	rs397508628
Map	rs397508628
PheGenI	rs397508628
Biobank	rs397508628
1000 genomes	rs397508628
hgdp	rs397508628
ensembl	rs397508628
geneview	rs397508628
scholar	rs397508628
google	rs397508628
pharmgkb	rs397508628
gwascentral	rs397508628
openSNP	rs397508628
23andMe	rs397508628
SNPshot	rs397508628
SNPdbe	rs397508628
MSV3d	rs397508628
GWAS Ctlg	rs397508628

Status

Merged into rs387906373

Max Magnitude

3

ClinVar
Risk
Alt
Reference	Rs397508628(TATT;TATT)
Significance	Pathogenic
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117292905_117292908delATTT
CLNSRC	CFTR2 OMIM Allelic Variant
CLNACC	RCV000047015.5,