List of variants in gene combination LOC126807546, SH3TC2 reported as benign for Susceptibility to mononeuropathy of the median nerve, mild

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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: 6

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HGVS	dbSNP	gnomAD frequency
NM_024577.4(SH3TC2):c.*19919T>C	rs2217638	0.77503
NM_024577.4(SH3TC2):c.*19573G>A	rs4560536	0.51021
NM_024577.4(SH3TC2):c.*20463T>C	rs77021631	0.16394
NM_024577.4(SH3TC2):c.*20166T>A	rs17795091	0.16389
NM_024577.4(SH3TC2):c.*20207C>T	rs114079860	0.01957
NM_024577.4(SH3TC2):c.*20142A>G	rs189978591	0.00313

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