rs3796619

Orientation

minus

Stabilized

minus

Make rs3796619(C;C)

Make rs3796619(C;T)

Make rs3796619(T;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

1101493

Gene

RNF212

is a	snp
is	mentioned by
dbSNP	rs3796619
dbSNP (classic)	rs3796619
ClinGen	rs3796619
ebi	rs3796619
HLI	rs3796619
Exac	rs3796619
Gnomad	rs3796619
Varsome	rs3796619
LitVar	rs3796619
Map	rs3796619
PheGenI	rs3796619
Biobank	rs3796619
1000 genomes	rs3796619
hgdp	rs3796619
ensembl	rs3796619
geneview	rs3796619
scholar	rs3796619
google	rs3796619
pharmgkb	rs3796619
gwascentral	rs3796619
openSNP	rs3796619
23andMe	rs3796619
SNPshot	rs3796619
SNPdbe	rs3796619
MSV3d	rs3796619
GWAS Ctlg	rs3796619

GMAF

0.4568

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

GWAS
SNP	rs3796619
PubMedID	[PMID 18239089]
Condition	Recombination rate (males)
Gene	RNF212,SPON2
Risk Allele	T
pValue	3.00E-024
OR	70.7
95% CI	84.3-57.1) cM decreas

OMIM	612042
Desc	RECOMBINATION RATE QUANTITATIVE TRAIT LOCUS 1; RRQTL1
Variant
Related	also

OMIM	612041
Desc	RING FINGER PROTEIN 212; RNF212
Variant
Related	also

OMIM	612041
Desc
Variant	0001
Related	also

[PMID 19002143] Sex-specific genetic architecture of human disease.

[PMID 19763160] Genetic analysis of variation in human meiotic recombination.

[PMID 20369022] Candidate causal regulatory effects by integration of expression QTLs with complex trait genetic associations.

ClinVar
Risk	rs3796619(C;C)
Alt	rs3796619(C;C)
Reference	rs3796619(T;T)
Significance	Other
Disease	Recombination rate quantitative trait locus 1
Variation	info
Gene	RNF212
CLNDBN	Recombination rate quantitative trait locus 1
Reversed	1
HGVS	NC_000004.11:g.1095281A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000000771.3,