List of variants in gene FOXH1, KIFC2 studied for Holoprosencephaly sequence

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_001369769.2(KIFC2):c.*616C>T	rs11781640	0.00421
NM_001369769.2(KIFC2):c.*775C>T	rs562738425	0.00075
NM_001369769.2(KIFC2):c.*377C>A	rs576710211	0.00052
NM_001369769.2(KIFC2):c.*794G>A	rs192907579	0.00031
NM_001369769.2(KIFC2):c.*538G>A	rs74360910	0.00024
NM_001369769.2(KIFC2):c.*761T>C	rs1024459830	0.00011
NM_001369769.2(KIFC2):c.*677G>C	rs148389554	0.00006
NM_001369769.2(KIFC2):c.*398G>A	rs886062751	0.00001
NM_001369769.2(KIFC2):c.*413C>T	rs1825046297	0.00001
NM_001369769.2(KIFC2):c.*467G>A	rs961808166	0.00001
NM_001369769.2(KIFC2):c.*419C>T	rs1825046517
NM_001369769.2(KIFC2):c.*426C>T	rs1362803083
NM_001369769.2(KIFC2):c.*495G>A	rs1825050087
NM_001369769.2(KIFC2):c.*527G>T	rs1440626432
NM_001369769.2(KIFC2):c.612_614del	rs550365735

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