List of variants in gene combination HRAS, LRRC56 reported as likely pathogenic for cardiomyopathy

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 27

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HGVS	dbSNP	gnomAD frequency
NM_005343.4(HRAS):c.36C>T (p.Gly12=)	rs727504424	0.00004
NM_005343.4(HRAS):c.171_185dup (p.Asp57_Gln61dup)	rs2133990973
NM_005343.4(HRAS):c.175G>A (p.Ala59Thr)	rs727503093
NM_005343.4(HRAS):c.175_176delinsCT (p.Ala59Leu)	rs727504747
NM_005343.4(HRAS):c.178G>A (p.Gly60Ser)	rs1589792804
NM_005343.4(HRAS):c.181C>A (p.Gln61Lys)	rs28933406
NM_005343.4(HRAS):c.181C>G (p.Gln61Glu)	rs28933406
NM_005343.4(HRAS):c.182A>C (p.Gln61Pro)	rs121913233
NM_005343.4(HRAS):c.182A>G (p.Gln61Arg)	rs121913233
NM_005343.4(HRAS):c.182A>T (p.Gln61Leu)	rs121913233
NM_005343.4(HRAS):c.183G>T (p.Gln61His)	rs121913496
NM_005343.4(HRAS):c.34G>A (p.Gly12Ser)	rs104894229
NM_005343.4(HRAS):c.34G>C (p.Gly12Arg)	rs104894229
NM_005343.4(HRAS):c.34G>T (p.Gly12Cys)	rs104894229
NM_005343.4(HRAS):c.35G>A (p.Gly12Asp)	rs104894230
NM_005343.4(HRAS):c.35G>C (p.Gly12Ala)	rs104894230
NM_005343.4(HRAS):c.35_36delinsAA (p.Gly12Glu)	rs727503094
NM_005343.4(HRAS):c.37G>A (p.Gly13Ser)	rs104894228
NM_005343.4(HRAS):c.37G>C (p.Gly13Arg)	rs104894228
NM_005343.4(HRAS):c.37G>T (p.Gly13Cys)	rs104894228
NM_005343.4(HRAS):c.38G>C (p.Gly13Ala)	rs104894226
NM_005343.4(HRAS):c.38G>T (p.Gly13Val)	rs104894226
NM_005343.4(HRAS):c.436G>A (p.Ala146Thr)	rs104894231
NM_005343.4(HRAS):c.436G>C (p.Ala146Pro)	rs104894231
NM_005343.4(HRAS):c.437C>T (p.Ala146Val)	rs121917759
NM_005343.4(HRAS):c.64C>A (p.Gln22Lys)	rs121917757
NM_176795.5(HRAS):c.488_497del (p.Leu163fs)	rs764755556

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