rs1057517131

Orientation

minus

Stabilized

minus

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

Make rs1057517131(-;TC)

Make rs1057517131(TC;TC)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

95249182

Gene

FANCC

is a	snp
is	mentioned by
dbSNP	rs1057517131
dbSNP (classic)	rs1057517131
ClinGen	rs1057517131
ebi	rs1057517131
HLI	rs1057517131
Exac	rs1057517131
Gnomad	rs1057517131
Varsome	rs1057517131
LitVar	rs1057517131
Map	rs1057517131
PheGenI	rs1057517131
Biobank	rs1057517131
1000 genomes	rs1057517131
hgdp	rs1057517131
ensembl	rs1057517131
geneview	rs1057517131
scholar	rs1057517131
google	rs1057517131
pharmgkb	rs1057517131
gwascentral	rs1057517131
openSNP	rs1057517131
23andMe	rs1057517131
SNPshot	rs1057517131
SNPdbe	rs1057517131
MSV3d	rs1057517131
GWAS Ctlg	rs1057517131

Max Magnitude

0

ClinVar
Risk	rs1057517131(TC;TC)
Alt	rs1057517131(TC;TC)
Reference	Rs1057517131(-;-)
Significance	Probable-Pathogenic
Disease	Fanconi anemia
Variation	info
Gene	FANCC
CLNDBN	Fanconi anemia, complementation group C
Reversed	1
HGVS	NC_000009.11:g.98011465_98011466dupGA
CLNSRC
CLNACC	RCV000409107.1,