rs587777894

Orientation

minus

Stabilized

minus

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

Make rs587777894(C;T)

Make rs587777894(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

11124516

Gene

MTOR

is a	snp
is	mentioned by
dbSNP	rs587777894
dbSNP (classic)	rs587777894
ClinGen	rs587777894
ebi	rs587777894
HLI	rs587777894
Exac	rs587777894
Gnomad	rs587777894
Varsome	rs587777894
LitVar	rs587777894
Map	rs587777894
PheGenI	rs587777894
Biobank	rs587777894
1000 genomes	rs587777894
hgdp	rs587777894
ensembl	rs587777894
geneview	rs587777894
scholar	rs587777894
google	rs587777894
pharmgkb	rs587777894
gwascentral	rs587777894
openSNP	rs587777894
23andMe	rs587777894
SNPshot	rs587777894
SNPdbe	rs587777894
MSV3d	rs587777894
GWAS Ctlg	rs587777894

Max Magnitude

0

ClinVar
Risk	rs587777894(A;A) rs587777894(T;T)
Alt	rs587777894(A;A) rs587777894(T;T)
Reference	Rs587777894(C;C)
Significance	Pathogenic
Disease	not provided Renal cell carcinoma Malignant melanoma of skin Papillary renal cell carcinoma Colorectal Neoplasms Glioblastoma Malignant neoplasm of body of uterus Uterine cervical neoplasms FOCAL CORTICAL DYSPLASIA Kidney Carcinoma
Variation	info
Gene	MTOR
CLNDBN	not provided Renal cell carcinoma Malignant melanoma of skin Papillary renal cell carcinoma, sporadic Colorectal Neoplasms Glioblastoma Malignant neoplasm of body of uterus Uterine cervical neoplasms FOCAL CORTICAL DYSPLASIA, TYPE II, SOMATIC Kidney Carcinoma
Reversed	1
HGVS	NC_000001.10:g.11184573G>A; NC_000001.10:g.11184573G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000190281.1, RCV000419624.1, RCV000422164.1, RCV000429373.1, RCV000430308.1, RCV000436863.1, RCV000439373.1, RCV000440054.1, RCV000477713.2, RCV000418200.1, RCV000420146.1, RCV000424789.1, RCV000428450.1, RCV000431294.1, RCV000435047.1, RCV000437777.1, RCV000441543.1, RCV000477715.2,