rs1057518066

Orientation

plus

Stabilized

plus

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

Make rs1057518066(C;T)

Make rs1057518066(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

135765732

Gene

KCNT1

is a	snp
is	mentioned by
dbSNP	rs1057518066
dbSNP (classic)	rs1057518066
ClinGen	rs1057518066
ebi	rs1057518066
HLI	rs1057518066
Exac	rs1057518066
Gnomad	rs1057518066
Varsome	rs1057518066
LitVar	rs1057518066
Map	rs1057518066
PheGenI	rs1057518066
Biobank	rs1057518066
1000 genomes	rs1057518066
hgdp	rs1057518066
ensembl	rs1057518066
geneview	rs1057518066
scholar	rs1057518066
google	rs1057518066
pharmgkb	rs1057518066
gwascentral	rs1057518066
openSNP	rs1057518066
23andMe	rs1057518066
SNPshot	rs1057518066
SNPdbe	rs1057518066
MSV3d	rs1057518066
GWAS Ctlg	rs1057518066

Max Magnitude

0

ClinVar
Risk	rs1057518066(T;T)
Alt	rs1057518066(T;T)
Reference	Rs1057518066(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	KCNT1
CLNDBN	not provided
Reversed	0
HGVS	NC_000009.11:g.138657578C>T
CLNSRC
CLNACC	RCV000413029.1,