rs121918303

Orientation

plus

Stabilized

plus

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

Make rs121918303(A;C)

Make rs121918303(C;C)

Reference

GRCh38 38.1/141

Chromosome

13

Position

31777398

Gene

RXFP2

is a	snp
is	mentioned by
dbSNP	rs121918303
dbSNP (classic)	rs121918303
ClinGen	rs121918303
ebi	rs121918303
HLI	rs121918303
Exac	rs121918303
Gnomad	rs121918303
Varsome	rs121918303
LitVar	rs121918303
Map	rs121918303
PheGenI	rs121918303
Biobank	rs121918303
1000 genomes	rs121918303
hgdp	rs121918303
ensembl	rs121918303
geneview	rs121918303
scholar	rs121918303
google	rs121918303
pharmgkb	rs121918303
gwascentral	rs121918303
openSNP	rs121918303
23andMe	rs121918303
SNPshot	rs121918303
SNPdbe	rs121918303
MSV3d	rs121918303
GWAS Ctlg	rs121918303

Merged from

Rs28939382

GMAF

0.001837

Max Magnitude

0

OMIM	606655
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121918303(C;C) rs121918303(G;G)
Alt	rs121918303(C;C) rs121918303(G;G)
Reference	Rs121918303(A;A)
Significance	Pathogenic
Disease	Cryptorchidism
Variation	info
Gene	RXFP2
CLNDBN	Cryptorchidism, unilateral or bilateral
Reversed	0
HGVS	NC_000013.10:g.32351535A>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000004376.3,