List of variants in gene combination SARM1, SLC46A1 reported as benign for digestive system disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 23

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HGVS	dbSNP	gnomAD frequency
NM_015077.4(SARM1):c.1924-1029G>A	rs1128161	0.59678
NM_015077.4(SARM1):c.1924-1133C>A	rs1128162	0.59676
NM_015077.4(SARM1):c.1924-279G>A	rs8079943	0.59408
NM_015077.4(SARM1):c.1924-196C>T	rs8081240	0.59034
NM_015077.4(SARM1):c.*1963G>A	rs2239908	0.58189
NM_015077.4(SARM1):c.*2442T>C	rs2239907	0.53216
NM_015077.4(SARM1):c.*308G>T	rs2239911	0.51926
NM_015077.4(SARM1):c.*517C>T	rs739439	0.12712
NM_015077.4(SARM1):c.*104C>T	rs73273104	0.03547
NM_015077.4(SARM1):c.1924-34A>G	rs117451747	0.02019
NM_015077.4(SARM1):c.*2641C>T	rs41297903	0.01106
NM_015077.4(SARM1):c.*624C>T	rs11871687	0.00541
NM_015077.4(SARM1):c.*1153T>C	rs41297923	0.00539
NM_015077.4(SARM1):c.*2127T>C	rs41297909	0.00501
NM_015077.4(SARM1):c.*1122A>G	rs8082600	0.00495
NM_015077.4(SARM1):c.*2678T>A	rs112801276	0.00456
NM_015077.4(SARM1):c.*527C>T	rs118138669	0.00108
NM_015077.4(SARM1):c.*1596T>C	rs2239909	0.00050
NM_015077.4(SARM1):c.*2699G>A	rs41297123	0.00026
NM_015077.4(SARM1):c.*361=	rs2239910
NM_015077.4(SARM1):c.*402G>A	rs12453383
NM_015077.4(SARM1):c.1924-833G>A	rs116278566
NM_015077.4(SARM1):c.1924-873dup	rs34879232

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