List of variants in gene LOC129935417, TMEM237 studied for autosomal recessive disease

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_001044385.3(TMEM237):c.9T>G (p.Thr3=)	rs6736435	0.02349
NM_001044385.3(TMEM237):c.-12G>A	rs113186360	0.01229
NM_001044385.3(TMEM237):c.-61G>A	rs571550977	0.00009
NM_001044385.3(TMEM237):c.33G>A (p.Glu11=)	rs544767440	0.00004
NM_001044385.3(TMEM237):c.15G>C (p.Ser5=)	rs879874108	0.00003
NM_001044385.3(TMEM237):c.1A>G (p.Met1Val)	rs957203033	0.00003
NM_001044385.3(TMEM237):c.22C>T (p.Arg8Trp)	rs972949531	0.00003
NM_001044385.3(TMEM237):c.-59G>A	rs886055449	0.00001
NM_001044385.3(TMEM237):c.-25G>A	rs568671275
NM_001044385.3(TMEM237):c.-67T>G	rs886055450
NM_001044385.3(TMEM237):c.14C>T (p.Ser5Leu)	rs562984785
NM_001044385.3(TMEM237):c.23G>A (p.Arg8Gln)	rs778373105
NM_001044385.3(TMEM237):c.24G>A (p.Arg8=)	rs377090903
NM_001044385.3(TMEM237):c.26T>A (p.Leu9Gln)	rs2105906100
NM_001044385.3(TMEM237):c.31G>A (p.Glu11Lys)	rs1319201699
NM_001044385.3(TMEM237):c.34G>A (p.Gly12Ser)

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