List of variants in gene RFWD3 studied for anemia

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_018124.4(RFWD3):c.269C>A (p.Thr90Asn)	rs8058922	0.72932
NM_018124.4(RFWD3):c.1212G>A (p.Thr404=)	rs4888262	0.58882
NM_018124.4(RFWD3):c.1755-33G>A	rs11149759	0.27669
NM_018124.4(RFWD3):c.1367G>C (p.Cys456Ser)	rs773701779	0.00001
NM_018124.4(RFWD3):c.2205G>A (p.Ser735=)	rs190386378	0.00001
NM_018124.4(RFWD3):c.1189G>C (p.Val397Leu)	rs1567572985
NM_018124.4(RFWD3):c.1577G>A (p.Ser526Asn)
NM_018124.4(RFWD3):c.1579C>A (p.Leu527Met)
NM_018124.4(RFWD3):c.1916T>A (p.Ile639Lys)	rs1555524842
NM_018124.4(RFWD3):c.204_205dup (p.Leu69fs)	rs1205970095

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