List of variants in gene SAMD13 studied for not specified

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001134663.2(SAMD13):c.122G>A (p.Arg41Gln)	rs370730440	0.00016
NM_001134663.2(SAMD13):c.-6C>T	rs200979305	0.00013
NM_001134663.2(SAMD13):c.3G>C (p.Met1Ile)	rs773163917	0.00011
NM_001134663.2(SAMD13):c.52A>C (p.Asn18His)	rs765037249	0.00001
NM_001134663.2(SAMD13):c.231A>T (p.Lys77Asn)	rs2526753620
NM_001134663.2(SAMD13):c.23A>C (p.Asn8Thr)
NM_001134663.2(SAMD13):c.47T>A (p.Val16Glu)
NM_001134663.2(SAMD13):c.71G>C (p.Arg24Thr)

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