rs587780835

Orientation

plus

Stabilized

plus

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

Make rs587780835(A;G)

Make rs587780835(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

58734116

Gene	LOC105371843, RAD51C

is a	snp
is	mentioned by
dbSNP	rs587780835
dbSNP (classic)	rs587780835
ClinGen	rs587780835
ebi	rs587780835
HLI	rs587780835
Exac	rs587780835
Gnomad	rs587780835
Varsome	rs587780835
LitVar	rs587780835
Map	rs587780835
PheGenI	rs587780835
Biobank	rs587780835
1000 genomes	rs587780835
hgdp	rs587780835
ensembl	rs587780835
geneview	rs587780835
scholar	rs587780835
google	rs587780835
pharmgkb	rs587780835
gwascentral	rs587780835
openSNP	rs587780835
23andMe	rs587780835
SNPshot	rs587780835
SNPdbe	rs587780835
MSV3d	rs587780835
GWAS Ctlg	rs587780835

Max Magnitude

0

ClinVar
Risk	rs587780835(G;G)
Alt	rs587780835(G;G)
Reference	Rs587780835(A;A)
Significance	Pathogenic
Disease	Fanconi anemia
Variation	info
Gene	RAD51C
CLNDBN	Fanconi anemia, complementation group O
Reversed	0
HGVS	NC_000017.10:g.56811477A>G
CLNSRC
CLNACC	RCV000123368.1,