rs587779898

Orientation

minus

Stabilized

minus

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

Make rs587779898(A;G)

Make rs587779898(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

9

Position

95249371

Gene

FANCC

is a	snp
is	mentioned by
dbSNP	rs587779898
dbSNP (classic)	rs587779898
ClinGen	rs587779898
ebi	rs587779898
HLI	rs587779898
Exac	rs587779898
Gnomad	rs587779898
Varsome	rs587779898
LitVar	rs587779898
Map	rs587779898
PheGenI	rs587779898
Biobank	rs587779898
1000 genomes	rs587779898
hgdp	rs587779898
ensembl	rs587779898
geneview	rs587779898
scholar	rs587779898
google	rs587779898
pharmgkb	rs587779898
gwascentral	rs587779898
openSNP	rs587779898
23andMe	rs587779898
SNPshot	rs587779898
SNPdbe	rs587779898
MSV3d	rs587779898
GWAS Ctlg	rs587779898

Max Magnitude

0

ClinVar
Risk	rs587779898(G;G)
Alt	rs587779898(G;G)
Reference	Rs587779898(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FANCC
CLNDBN	not provided
Reversed	1
HGVS	NC_000009.11:g.98011653T>C
CLNSRC
CLNACC	RCV000115337.3,