RS1670533 RNF212

Health Risk Chr 4:1084398 snv intron variant

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What This Variant Does

"[OMIM:RING FINGER PROTEIN 212

Associated Conditions

RECOMBINATION RATE QUANTITATIVE TRAIT LOCUS 1

GWAS Studies (1)

Trait	Risk Allele	OR / Beta	P-value	Study
Recombination rate (females)	C	OR: 88.2	2E-12	PubMed

Population Frequencies

1kG AFR

3.6%

1kG ALL

22.7%

1kG AMR

34.9%

1kG EAS

64.9%

1kG EUR

24.4%

1kG SAS

74.8%

Other Variants in RNF212