rs370974124

Orientation

plus

Stabilized

plus

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

Make rs370974124(A;A)

Make rs370974124(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

9

Position

95101721

Gene	C9orf3, FANCC

is a	snp
is	mentioned by
dbSNP	rs370974124
dbSNP (classic)	rs370974124
ClinGen	rs370974124
ebi	rs370974124
HLI	rs370974124
Exac	rs370974124
Gnomad	rs370974124
Varsome	rs370974124
LitVar	rs370974124
Map	rs370974124
PheGenI	rs370974124
Biobank	rs370974124
1000 genomes	rs370974124
hgdp	rs370974124
ensembl	rs370974124
geneview	rs370974124
scholar	rs370974124
google	rs370974124
pharmgkb	rs370974124
gwascentral	rs370974124
openSNP	rs370974124
23andMe	rs370974124
SNPshot	rs370974124
SNPdbe	rs370974124
MSV3d	rs370974124
GWAS Ctlg	rs370974124

Max Magnitude

0

ClinVar
Risk	rs370974124(A;A) rs370974124(T;T)
Alt	rs370974124(A;A) rs370974124(T;T)
Reference	Rs370974124(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	FANCC
CLNDBN	not provided
Reversed	0
HGVS	NC_000009.11:g.97864003G>A
CLNSRC
CLNACC	RCV000218828.2,