rs139027297

Orientation

plus

Stabilized

plus

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

Make rs139027297(A;T)

Make rs139027297(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

9

Position

2718517

Gene

KCNV2

is a	snp
is	mentioned by
dbSNP	rs139027297
dbSNP (classic)	rs139027297
ClinGen	rs139027297
ebi	rs139027297
HLI	rs139027297
Exac	rs139027297
Gnomad	rs139027297
Varsome	rs139027297
LitVar	rs139027297
Map	rs139027297
PheGenI	rs139027297
Biobank	rs139027297
1000 genomes	rs139027297
hgdp	rs139027297
ensembl	rs139027297
geneview	rs139027297
scholar	rs139027297
google	rs139027297
pharmgkb	rs139027297
gwascentral	rs139027297
openSNP	rs139027297
23andMe	rs139027297
SNPshot	rs139027297
SNPdbe	rs139027297
MSV3d	rs139027297
GWAS Ctlg	rs139027297

Max Magnitude

0

ClinVar
Risk	rs139027297(G;G) rs139027297(T;T)
Alt	rs139027297(G;G) rs139027297(T;T)
Reference	Rs139027297(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KCNV2
CLNDBN	not provided
Reversed	0
HGVS	NC_000009.11:g.2718517A>T
CLNSRC
CLNACC	RCV000255665.1,