List of variants in gene RAB7A reported as benign for Charcot-Marie-Tooth disease type 2

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_004637.6(RAB7A):c.*863C>G	rs59753334	0.06155
NM_004637.6(RAB7A):c.*189A>G	rs11549750	0.05501
NM_004637.6(RAB7A):c.219C>T (p.Leu73=)	rs4548	0.04279
NM_004637.6(RAB7A):c.*997T>C	rs3755593	0.03614
NM_004637.6(RAB7A):c.*206G>A	rs16851333	0.01808
NM_004637.6(RAB7A):c.-97C>G	rs141622970	0.01485
NM_004637.6(RAB7A):c.-29G>T	rs112000804	0.01334
NM_004637.6(RAB7A):c.*163T>G	rs182521602	0.00395
NM_004637.6(RAB7A):c.495G>A (p.Ala165=)	rs146566121	0.00341
NM_004637.6(RAB7A):c.423C>G (p.Ala141=)	rs61758751	0.00210
NM_004637.6(RAB7A):c.87G>A (p.Val29=)	rs145441548	0.00039
NM_004637.6(RAB7A):c.*625T>C	rs545004919	0.00025
NM_004637.5(RAB7A):c.-215C>T	rs560785742	0.00022
NM_004637.6(RAB7A):c.-115C>T	rs374777610	0.00009
NM_004637.6(RAB7A):c.*1374G>A	rs539522952	0.00003
NM_004637.6(RAB7A):c.*229C>T	rs147244704
NM_004637.6(RAB7A):c.*846A>G	rs532629721

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