rs1057523641

Orientation

plus

Stabilized

plus

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

Make rs1057523641(C;C)

Make rs1057523641(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

135784535

Gene	KCNT1, LOC107987139

is a	snp
is	mentioned by
dbSNP	rs1057523641
dbSNP (classic)	rs1057523641
ClinGen	rs1057523641
ebi	rs1057523641
HLI	rs1057523641
Exac	rs1057523641
Gnomad	rs1057523641
Varsome	rs1057523641
LitVar	rs1057523641
Map	rs1057523641
PheGenI	rs1057523641
Biobank	rs1057523641
1000 genomes	rs1057523641
hgdp	rs1057523641
ensembl	rs1057523641
geneview	rs1057523641
scholar	rs1057523641
google	rs1057523641
pharmgkb	rs1057523641
gwascentral	rs1057523641
openSNP	rs1057523641
23andMe	rs1057523641
SNPshot	rs1057523641
SNPdbe	rs1057523641
MSV3d	rs1057523641
GWAS Ctlg	rs1057523641

Max Magnitude

0

ClinVar
Risk	rs1057523641(C;C)
Alt	rs1057523641(C;C)
Reference	Rs1057523641(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	KCNT1
CLNDBN	not provided
Reversed	0
HGVS	NC_000009.11:g.138676381T>C
CLNSRC
CLNACC	RCV000443900.1,