rs1057522978

Orientation

plus

Stabilized

plus

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

Make rs1057522978(A;G)

Make rs1057522978(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

135770972

Gene

KCNT1

is a	snp
is	mentioned by
dbSNP	rs1057522978
dbSNP (classic)	rs1057522978
ClinGen	rs1057522978
ebi	rs1057522978
HLI	rs1057522978
Exac	rs1057522978
Gnomad	rs1057522978
Varsome	rs1057522978
LitVar	rs1057522978
Map	rs1057522978
PheGenI	rs1057522978
Biobank	rs1057522978
1000 genomes	rs1057522978
hgdp	rs1057522978
ensembl	rs1057522978
geneview	rs1057522978
scholar	rs1057522978
google	rs1057522978
pharmgkb	rs1057522978
gwascentral	rs1057522978
openSNP	rs1057522978
23andMe	rs1057522978
SNPshot	rs1057522978
SNPdbe	rs1057522978
MSV3d	rs1057522978
GWAS Ctlg	rs1057522978

Max Magnitude

0

ClinVar
Risk	rs1057522978(G;G)
Alt	rs1057522978(G;G)
Reference	Rs1057522978(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	KCNT1
CLNDBN	not provided
Reversed	0
HGVS	NC_000009.11:g.138662818A>G
CLNSRC
CLNACC	RCV000425973.1,