rs1057519366

Orientation

minus

Stabilized

minus

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

Make rs1057519366(-;C)

Make rs1057519366(C;C)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

95150013

Gene

FANCC

is a	snp
is	mentioned by
dbSNP	rs1057519366
dbSNP (classic)	rs1057519366
ClinGen	rs1057519366
ebi	rs1057519366
HLI	rs1057519366
Exac	rs1057519366
Gnomad	rs1057519366
Varsome	rs1057519366
LitVar	rs1057519366
Map	rs1057519366
PheGenI	rs1057519366
Biobank	rs1057519366
1000 genomes	rs1057519366
hgdp	rs1057519366
ensembl	rs1057519366
geneview	rs1057519366
scholar	rs1057519366
google	rs1057519366
pharmgkb	rs1057519366
gwascentral	rs1057519366
openSNP	rs1057519366
23andMe	rs1057519366
SNPshot	rs1057519366
SNPdbe	rs1057519366
MSV3d	rs1057519366
GWAS Ctlg	rs1057519366

Max Magnitude

0

ClinVar
Risk	rs1057519366(C;C)
Alt	rs1057519366(C;C)
Reference	Rs1057519366(-;-)
Significance	Probable-Pathogenic
Disease	Carcinoma of colon
Variation	info
Gene	FANCC
CLNDBN	Carcinoma of colon
Reversed	1
HGVS	NC_000009.11:g.97912296dupG
CLNSRC
CLNACC	RCV000416810.1,