rs770637624

Orientation

plus

Stabilized

plus

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

Make rs770637624(C;T)

Make rs770637624(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

58709862

Gene

RAD51C

is a	snp
is	mentioned by
dbSNP	rs770637624
dbSNP (classic)	rs770637624
ClinGen	rs770637624
ebi	rs770637624
HLI	rs770637624
Exac	rs770637624
Gnomad	rs770637624
Varsome	rs770637624
LitVar	rs770637624
Map	rs770637624
PheGenI	rs770637624
Biobank	rs770637624
1000 genomes	rs770637624
hgdp	rs770637624
ensembl	rs770637624
geneview	rs770637624
scholar	rs770637624
google	rs770637624
pharmgkb	rs770637624
gwascentral	rs770637624
openSNP	rs770637624
23andMe	rs770637624
SNPshot	rs770637624
SNPdbe	rs770637624
MSV3d	rs770637624
GWAS Ctlg	rs770637624

Max Magnitude

0

ClinVar
Risk	rs770637624(T;T)
Alt	rs770637624(T;T)
Reference	Rs770637624(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Fanconi anemia not provided
Variation	info
Gene	RAD51C
CLNDBN	Hereditary cancer-predisposing syndrome Fanconi anemia, complementation group O not provided
Reversed	0
HGVS	NC_000017.10:g.56787223C>T
CLNSRC
CLNACC	RCV000165947.3, RCV000233212.2, RCV000484844.1,