rs769039987

Orientation

plus

Stabilized

plus

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

Make rs769039987(A;A)

Make rs769039987(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

9

Position

95150074

Gene

FANCC

is a	snp
is	mentioned by
dbSNP	rs769039987
dbSNP (classic)	rs769039987
ClinGen	rs769039987
ebi	rs769039987
HLI	rs769039987
Exac	rs769039987
Gnomad	rs769039987
Varsome	rs769039987
LitVar	rs769039987
Map	rs769039987
PheGenI	rs769039987
Biobank	rs769039987
1000 genomes	rs769039987
hgdp	rs769039987
ensembl	rs769039987
geneview	rs769039987
scholar	rs769039987
google	rs769039987
pharmgkb	rs769039987
gwascentral	rs769039987
openSNP	rs769039987
23andMe	rs769039987
SNPshot	rs769039987
SNPdbe	rs769039987
MSV3d	rs769039987
GWAS Ctlg	rs769039987

Max Magnitude

0

ClinVar
Risk	rs769039987(A;A)
Alt	rs769039987(A;A)
Reference	Rs769039987(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	FANCC
CLNDBN	not provided
Reversed	0
HGVS	NC_000009.11:g.97912356G>A
CLNSRC
CLNACC	RCV000224844.1,