rs730881940

Orientation

plus

Stabilized

plus

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

Make rs730881940(-;A)

Make rs730881940(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

58695179

Gene

RAD51C

is a	snp
is	mentioned by
dbSNP	rs730881940
dbSNP (classic)	rs730881940
ClinGen	rs730881940
ebi	rs730881940
HLI	rs730881940
Exac	rs730881940
Gnomad	rs730881940
Varsome	rs730881940
LitVar	rs730881940
Map	rs730881940
PheGenI	rs730881940
Biobank	rs730881940
1000 genomes	rs730881940
hgdp	rs730881940
ensembl	rs730881940
geneview	rs730881940
scholar	rs730881940
google	rs730881940
pharmgkb	rs730881940
gwascentral	rs730881940
openSNP	rs730881940
23andMe	rs730881940
SNPshot	rs730881940
SNPdbe	rs730881940
MSV3d	rs730881940
GWAS Ctlg	rs730881940

Max Magnitude

0

ClinVar
Risk	rs730881940(A;A)
Alt	rs730881940(A;A)
Reference	Rs730881940(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Fanconi anemia
Variation	info
Gene	RAD51C
CLNDBN	Hereditary cancer-predisposing syndrome Fanconi anemia, complementation group O
Reversed	0
HGVS	NC_000017.10:g.56772540dupA
CLNSRC
CLNACC	RCV000160934.1, RCV000465754.1,