List of variants in gene PIGG reported as benign for developmental disorder of mental health

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 38

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HGVS	dbSNP	gnomAD frequency
NM_001127178.3(PIGG):c.2261+49A>T	rs7697650	0.97007
NM_001127178.3(PIGG):c.571-563A>G	rs4690182	0.87699
NM_001127178.3(PIGG):c.1989C>T (p.Ala663=)	rs13150531	0.19173
NM_001127178.3(PIGG):c.1828T>C (p.Cys610Arg)	rs7666425	0.19169
NM_001127178.3(PIGG):c.1743T>C (p.Leu581=)	rs7666226	0.19160
NM_001127178.3(PIGG):c.2795T>C (p.Phe932Ser)	rs1127410	0.19048
NM_001127178.3(PIGG):c.2642T>C (p.Ile881Thr)	rs34623004	0.18986
NM_001127178.3(PIGG):c.2095G>A (p.Val699Ile)	rs13114026	0.15552
NM_001127178.3(PIGG):c.1373G>A (p.Arg458His)	rs13115344	0.13254
NM_001127178.3(PIGG):c.2191G>A (p.Val731Ile)	rs34916638	0.03501
NM_001127178.3(PIGG):c.990T>C (p.Ser330=)	rs11726338	0.02569
NM_001127178.3(PIGG):c.1967C>T (p.Ala656Val)	rs61749092	0.01599
NM_001127178.3(PIGG):c.158C>A (p.Ala53Asp)	rs28454778	0.00937
NM_001127178.3(PIGG):c.2069+16C>T	rs144533568	0.00716
NM_001127178.3(PIGG):c.1520C>T (p.Ala507Val)	rs144879126	0.00498
NM_001127178.3(PIGG):c.1930G>A (p.Glu644Lys)	rs114931121	0.00498
NM_001127178.3(PIGG):c.759+16G>A	rs148792489	0.00426
NM_001127178.3(PIGG):c.771G>A (p.Thr257=)	rs35496504	0.00322
NM_001127178.3(PIGG):c.1114+8A>G	rs182522437	0.00233
NM_001127178.3(PIGG):c.1254G>A (p.Thr418=)	rs139518242	0.00227
NM_001127178.3(PIGG):c.1581C>T (p.Thr527=)	rs143989093	0.00179
NM_001127178.3(PIGG):c.1114+15C>T	rs200262444	0.00170
NM_001127178.3(PIGG):c.1114+9A>G	rs150974506	0.00159
NM_001127178.3(PIGG):c.902-16G>A	rs187291662	0.00157
NM_001127178.3(PIGG):c.2150C>A (p.Ser717Tyr)	rs117059276	0.00137
NM_001127178.3(PIGG):c.2085C>T (p.Ala695=)	rs150774662	0.00112
NM_001127178.3(PIGG):c.2279G>A (p.Arg760His)	rs200170221	0.00022
NM_001127178.3(PIGG):c.588G>A (p.Thr196=)	rs149455987	0.00020
NM_001127178.3(PIGG):c.1594G>C (p.Gly532Arg)	rs781714196	0.00012
NM_001127178.3(PIGG):c.2769C>T (p.Tyr923=)	rs148579497	0.00012
NM_001127178.3(PIGG):c.361-8G>T	rs575862015	0.00004
NM_001127178.3(PIGG):c.883G>T (p.Ala295Ser)	rs201853289	0.00004
NM_001127178.3(PIGG):c.154+11dup	rs782776784
NM_001127178.3(PIGG):c.1614+9G>A	rs188737876
NM_001127178.3(PIGG):c.1614+9G>C	rs188737876
NM_001127178.3(PIGG):c.164C>A (p.Ser55Tyr)	rs34120878
NM_001127178.3(PIGG):c.2069+9G>T	rs149305291
NM_001127178.3(PIGG):c.759+13G>A	rs201035016

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