rs730881931

Orientation

plus

Stabilized

plus

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

Make rs730881931(C;C)

Make rs730881931(C;T)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

58695191

Gene

RAD51C

is a	snp
is	mentioned by
dbSNP	rs730881931
dbSNP (classic)	rs730881931
ClinGen	rs730881931
ebi	rs730881931
HLI	rs730881931
Exac	rs730881931
Gnomad	rs730881931
Varsome	rs730881931
LitVar	rs730881931
Map	rs730881931
PheGenI	rs730881931
Biobank	rs730881931
1000 genomes	rs730881931
hgdp	rs730881931
ensembl	rs730881931
geneview	rs730881931
scholar	rs730881931
google	rs730881931
pharmgkb	rs730881931
gwascentral	rs730881931
openSNP	rs730881931
23andMe	rs730881931
SNPshot	rs730881931
SNPdbe	rs730881931
MSV3d	rs730881931
GWAS Ctlg	rs730881931

Max Magnitude

0

ClinVar
Risk	rs730881931(C;C)
Alt	rs730881931(C;C)
Reference	Rs730881931(T;T)
Significance	Probable-Pathogenic
Disease	not provided Hereditary cancer-predisposing syndrome Fanconi anemia
Variation	info
Gene	RAD51C
CLNDBN	not provided Hereditary cancer-predisposing syndrome Fanconi anemia, complementation group O
Reversed	0
HGVS	NC_000017.10:g.56772552T>C
CLNSRC
CLNACC	RCV000160923.2, RCV000221514.1, RCV000467500.1,