rs267606997

Orientation

plus

Stabilized

plus

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

Make rs267606997(A;A)

Make rs267606997(A;G)

Reference

GRCh38 38.1/141

Chromosome

17

Position

58709926

Gene

RAD51C

is a	snp
is	mentioned by
dbSNP	rs267606997
dbSNP (classic)	rs267606997
ClinGen	rs267606997
ebi	rs267606997
HLI	rs267606997
Exac	rs267606997
Gnomad	rs267606997
Varsome	rs267606997
LitVar	rs267606997
Map	rs267606997
PheGenI	rs267606997
Biobank	rs267606997
1000 genomes	rs267606997
hgdp	rs267606997
ensembl	rs267606997
geneview	rs267606997
scholar	rs267606997
google	rs267606997
pharmgkb	rs267606997
gwascentral	rs267606997
openSNP	rs267606997
23andMe	rs267606997
SNPshot	rs267606997
SNPdbe	rs267606997
MSV3d	rs267606997
GWAS Ctlg	rs267606997

Max Magnitude

0

ClinVar
Risk	rs267606997(A;A)
Alt	rs267606997(A;A)
Reference	Rs267606997(G;G)
Significance	Other
Disease	Fanconi anemia Hereditary cancer-predisposing syndrome
Variation	info
Gene	RAD51C
CLNDBN	Fanconi anemia, complementation group O Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000017.10:g.56787287G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000007224.2, RCV000131703.2,