List of variants in gene combination DSG1, DSG4 reported as benign for alopecia

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_177986.5(DSG4):c.1930A>C (p.Ile644Leu)	rs4799570	0.93107
NM_177986.5(DSG4):c.495C>T (p.Ser165=)	rs9956865	0.78725
NM_177986.5(DSG4):c.3066C>A (p.Pro1022=)	rs7234288	0.72694
NM_177986.5(DSG4):c.258G>A (p.Arg86=)	rs16959856	0.70447
NM_177986.5(DSG4):c.2748A>G (p.Pro916=)	rs12960081	0.40506
NM_177986.5(DSG4):c.*31C>T	rs7234333	0.15278
NM_177986.5(DSG4):c.30C>T (p.Cys10=)	rs36101975	0.13937
NM_177986.5(DSG4):c.1604T>C (p.Ile535Thr)	rs7229252	0.01924
NM_177986.5(DSG4):c.2391A>C (p.Arg797=)	rs112653254	0.01253
NM_177986.5(DSG4):c.2796T>G (p.Asn932Lys)	rs373510855	0.00007

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