List of variants in gene CRYAB reported by Fulgent Genetics, Fulgent Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_001289808.2(CRYAB):c.37C>A (p.Pro13Thr)	rs1349139935	0.00006
NM_001289808.2(CRYAB):c.367C>T (p.Arg123Trp)	rs534473091	0.00005
NM_001289808.2(CRYAB):c.470G>A (p.Arg157His)	rs141638421	0.00005
NM_001289808.2(CRYAB):c.275A>G (p.Lys92Arg)	rs1256600488	0.00004
NM_001289808.2(CRYAB):c.115C>G (p.Pro39Ala)	rs145768025	0.00003
NM_001289808.2(CRYAB):c.119C>T (p.Thr40Met)	rs782122417	0.00003
NM_001289808.2(CRYAB):c.65G>A (p.Arg22His)	rs782316391	0.00003
NM_001289808.2(CRYAB):c.102G>T (p.Glu34Asp)	rs886047688	0.00001
NM_001289808.2(CRYAB):c.343del (p.Ser115fs)	rs281865142	0.00001
NM_001289808.2(CRYAB):c.362A>G (p.Lys121Arg)	rs781915800	0.00001
NM_001289808.2(CRYAB):c.115C>T (p.Pro39Ser)	rs145768025
NM_001289808.2(CRYAB):c.16C>T (p.His6Tyr)	rs794728982
NM_001289808.2(CRYAB):c.319C>T (p.Arg107Cys)	rs782520163
NM_001289808.2(CRYAB):c.31C>G (p.Arg11Gly)	rs781902168
NM_001289808.2(CRYAB):c.324+13dup	rs782303631

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