List of variants in gene HSPA9 studied for bone disorder

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_004134.7(HSPA9):c.1933C>T (p.Leu645=)	rs10117	0.51956
NM_004134.7(HSPA9):c.21T>G (p.Ala7=)	rs36043650	0.00380
NM_004134.7(HSPA9):c.882_883del (p.Gly295_Val296insTer)	rs772570880	0.00006
NM_004134.7(HSPA9):c.967G>A (p.Val323Met)	rs149041674	0.00005
NM_004134.7(HSPA9):c.1178C>G (p.Pro393Arg)	rs754137313	0.00003
NM_004134.7(HSPA9):c.376C>T (p.Arg126Trp)	rs751478142	0.00001
NM_004134.7(HSPA9):c.1994C>A (p.Ser665Tyr)
NM_004134.7(HSPA9):c.383A>G (p.Tyr128Cys)	rs765368797
NM_004134.7(HSPA9):c.599C>T (p.Ser200Leu)
NM_004134.7(HSPA9):c.717-17del	rs71574426

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