rs397514688

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs397514688(C;T)

Make rs397514688(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

63483172

Gene

ACE

is a	snp
is	mentioned by
dbSNP	rs397514688
dbSNP (classic)	rs397514688
ClinGen	rs397514688
ebi	rs397514688
HLI	rs397514688
Exac	rs397514688
Gnomad	rs397514688
Varsome	rs397514688
LitVar	rs397514688
Map	rs397514688
PheGenI	rs397514688
Biobank	rs397514688
1000 genomes	rs397514688
hgdp	rs397514688
ensembl	rs397514688
geneview	rs397514688
scholar	rs397514688
google	rs397514688
pharmgkb	rs397514688
gwascentral	rs397514688
openSNP	rs397514688
23andMe	rs397514688
SNPshot	rs397514688
SNPdbe	rs397514688
MSV3d	rs397514688
GWAS Ctlg	rs397514688

Max Magnitude

0

ClinVar
Risk	rs397514688(T;T)
Alt	rs397514688(T;T)
Reference	Rs397514688(C;C)
Significance	Pathogenic
Disease	Renal dysplasia not provided
Variation	info
Gene	ACE
CLNDBN	Renal dysplasia not provided
Reversed	0
HGVS	NC_000017.10:g.61560533C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000043470.25, RCV000321927.1,