rs797044884

Orientation

plus

Stabilized

plus

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

Make rs797044884(-;GA)

Make rs797044884(GA;GA)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

59677130

Gene

CLTC

is a	snp
is	mentioned by
dbSNP	rs797044884
ClinGen	rs797044884
ebi	rs797044884
HLI	rs797044884
Exac	rs797044884
Varsome	rs797044884
Map	rs797044884
PheGenI	rs797044884
hapmap	rs797044884
1000 genomes	rs797044884
hgdp	rs797044884
ensembl	rs797044884
gopubmed	rs797044884
geneview	rs797044884
scholar	rs797044884
google	rs797044884
pharmgkb	rs797044884
gwascentral	rs797044884
openSNP	rs797044884
23andMe	rs797044884
23andMe all	rs797044884
SNP Nexus
SNPshot	rs797044884
SNPdbe	rs797044884
MSV3d	rs797044884
GWAS Ctlg	rs797044884

Max Magnitude

0

ClinVar
Risk	rs797044884(AG;AG)
Alt	rs797044884(AG;AG)
Reference	Rs797044884(-;-)
Significance	Probable-Pathogenic
Disease	Inborn genetic diseases
Variation	info
Gene	CLTC
CLNDBN	Inborn genetic diseases
Reversed	0
HGVS	NC_000017.10:g.57754490_57754491dupGA
CLNSRC
CLNACC	RCV000190705.1,