rs371897078

Orientation

plus

Stabilized

plus

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

Make rs371897078(C;T)

Make rs371897078(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

95111630

Gene	C9orf3, FANCC

is a	snp
is	mentioned by
dbSNP	rs371897078
dbSNP (classic)	rs371897078
ClinGen	rs371897078
ebi	rs371897078
HLI	rs371897078
Exac	rs371897078
Gnomad	rs371897078
Varsome	rs371897078
LitVar	rs371897078
Map	rs371897078
PheGenI	rs371897078
Biobank	rs371897078
1000 genomes	rs371897078
hgdp	rs371897078
ensembl	rs371897078
geneview	rs371897078
scholar	rs371897078
google	rs371897078
pharmgkb	rs371897078
gwascentral	rs371897078
openSNP	rs371897078
23andMe	rs371897078
SNPshot	rs371897078
SNPdbe	rs371897078
MSV3d	rs371897078
GWAS Ctlg	rs371897078

Max Magnitude

0

ClinVar
Risk	rs371897078(A;A) rs371897078(T;T)
Alt	rs371897078(A;A) rs371897078(T;T)
Reference	Rs371897078(C;C)
Significance	Pathogenic
Disease	not provided Fanconi anemia Fanconi anemia not specified
Variation	info
Gene	FANCC
CLNDBN	not provided Fanconi anemia, complementation group C Fanconi anemia not specified
Reversed	0
HGVS	NC_000009.11:g.97873912C>A; NC_000009.11:g.97873912C>T
CLNSRC
CLNACC	RCV000202668.1, RCV000409441.1, RCV000205129.1, RCV000484234.1,