rs759900071

Orientation

plus

Stabilized

plus

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

Make rs759900071(A;A)

Make rs759900071(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

95117318

Gene	C9orf3, FANCC

is a	snp
is	mentioned by
dbSNP	rs759900071
dbSNP (classic)	rs759900071
ClinGen	rs759900071
ebi	rs759900071
HLI	rs759900071
Exac	rs759900071
Gnomad	rs759900071
Varsome	rs759900071
LitVar	rs759900071
Map	rs759900071
PheGenI	rs759900071
Biobank	rs759900071
1000 genomes	rs759900071
hgdp	rs759900071
ensembl	rs759900071
geneview	rs759900071
scholar	rs759900071
google	rs759900071
pharmgkb	rs759900071
gwascentral	rs759900071
openSNP	rs759900071
23andMe	rs759900071
SNPshot	rs759900071
SNPdbe	rs759900071
MSV3d	rs759900071
GWAS Ctlg	rs759900071

Max Magnitude

0

ClinVar
Risk	rs759900071(A;A) rs759900071(C;C)
Alt	rs759900071(A;A) rs759900071(C;C)
Reference	Rs759900071(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FANCC
CLNDBN	not provided
Reversed	0
HGVS	NC_000009.11:g.97879600G>A
CLNSRC
CLNACC	RCV000483955.1,