ClinVar Miner

List of variants in gene combination HBG2, LOC106099065 reported as other

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Total variants: 31
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HGVS dbSNP
NM_000184.2(HBG2):c.103G>A (p.Val35Ile) rs35885783
NM_000184.2(HBG2):c.121A>G (p.Arg41Gly) rs34532478
NM_000184.2(HBG2):c.122G>A (p.Arg41Lys) rs281864892
NM_000184.2(HBG2):c.167T>G (p.Met56Arg) rs34915311
NM_000184.2(HBG2):c.178A>G (p.Lys60Glu) rs28933078
NM_000184.2(HBG2):c.17A>G (p.Glu6Gly) rs34263826
NM_000184.2(HBG2):c.199A>C (p.Lys67Gln) rs34264694
NM_000184.2(HBG2):c.200A>G (p.Lys67Arg) rs35481866
NM_000184.2(HBG2):c.22G>A (p.Asp8Asn) rs34501593
NM_000184.2(HBG2):c.233A>G (p.His78Arg) rs34150306
NM_000184.2(HBG2):c.241G>A (p.Asp81Asn) rs63751148
NM_000184.2(HBG2):c.283G>A (p.Asp95Asn) rs35812514
NM_000184.2(HBG2):c.304G>A (p.Glu102Lys) rs34876238
NM_000184.2(HBG2):c.38C>G (p.Thr13Arg) rs281864890
NM_000184.2(HBG2):c.49G>C (p.Gly17Arg) rs34907654
NM_000184.2(HBG2):c.4G>T (p.Gly2Cys) rs36006195
NM_000184.2(HBG2):c.68A>G (p.Asp23Gly) rs281864891
NM_000184.2(HBG2):c.68A>T (p.Asp23Val) rs281864891
NM_000184.2(HBG2):c.79G>A (p.Glu27Lys) rs35654328
NM_000184.3(HBG2):c.133A>C (p.Ser45Arg) rs34017450
NM_000184.3(HBG2):c.178A>C (p.Lys60Gln) rs28933078
NM_000184.3(HBG2):c.198G>C (p.Lys66Asn) rs34019507
NM_000184.3(HBG2):c.217G>C (p.Gly73Arg) rs281860594
NM_000184.3(HBG2):c.227T>C (p.Ile76Thr) rs104894225
NM_000184.3(HBG2):c.25A>C (p.Lys9Gln) rs35521813
NM_000184.3(HBG2):c.315G>C (p.Lys105Asn) rs35717854
NM_000184.3(HBG2):c.46T>C (p.Trp16Arg) rs34438981
NM_000184.3(HBG2):c.54G>C (p.Lys18Asn) rs35621390
NM_000184.3(HBG2):c.60T>A (p.Asn20Lys) rs34018799
NM_000184.3(HBG2):c.64G>C (p.Glu22Gln) rs33955330
NM_000184.3(HBG2):c.77G>A (p.Gly26Glu) rs35687396

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