Name: rs3078036
Published: September 21, 2022
License: Open Access

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs3078036

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr12:120763874-120763884 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: delAAA / delAA / delA / dupA / dup…
delAAA / delAA / delA / dupA / dupAA
Variation Type: Indel Insertion and Deletion
Frequency: (A)₁₁=0.4725 (1821/3854, ALSPAC)
(A)₁₁=0.2543 (853/3354, 1000G)
delAAA=0.0000 (0/1094, ALFA) (+ 4 more)
delAA=0.0000 (0/1094, ALFA)
delA=0.0000 (0/1094, ALFA)
dupA=0.0000 (0/1094, ALFA)
dupAA=0.0000 (0/1094, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SPPL3 : 3 Prime UTR Variant
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	1094	AAAAAAAAAAA=1.0000	AAAAAAAA=0.0000, AAAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
European	Sub	1008	AAAAAAAAAAA=1.0000	AAAAAAAA=0.0000, AAAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
African	Sub	36	AAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African Others	Sub	0	AAAAAAAAAAA=0	AAAAAAAA=0, AAAAAAAAA=0, AAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0	0	0	0	N/A
African American	Sub	36	AAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Asian	Sub	4	AAAAAAAAAAA=1.0	AAAAAAAA=0.0, AAAAAAAAA=0.0, AAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	2	AAAAAAAAAAA=1.0	AAAAAAAA=0.0, AAAAAAAAA=0.0, AAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	2	AAAAAAAAAAA=1.0	AAAAAAAA=0.0, AAAAAAAAA=0.0, AAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	10	AAAAAAAAAAA=1.0	AAAAAAAA=0.0, AAAAAAAAA=0.0, AAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	12	AAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	0	AAAAAAAAAAA=0	AAAAAAAA=0, AAAAAAAAA=0, AAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0	0	0	0	N/A
Other	Sub	24	AAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	(A)₁₁=0.4725	delAA=0.5275
1000Genomes	Global	Study-wide	3354	(A)₁₁=0.2543	delAA=0.7457
1000Genomes	Europe	Sub	865	(A)₁₁=0.407	delAA=0.593
1000Genomes	African	Sub	701	(A)₁₁=0.106	delAA=0.894
1000Genomes	South Asian	Sub	670	(A)₁₁=0.260	delAA=0.740
1000Genomes	East Asian	Sub	561	(A)₁₁=0.221	delAA=0.779
1000Genomes	American	Sub	557	(A)₁₁=0.232	delAA=0.768
Allele Frequency Aggregator	Total	Global	1094	(A)₁₁=1.0000	delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	European	Sub	1008	(A)₁₁=1.0000	delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	African	Sub	36	(A)₁₁=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Other	Sub	24	(A)₁₁=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Latin American 2	Sub	12	(A)₁₁=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Latin American 1	Sub	10	(A)₁₁=1.0	delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0
Allele Frequency Aggregator	Asian	Sub	4	(A)₁₁=1.0	delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0
Allele Frequency Aggregator	South Asian	Sub	0	(A)₁₁=0	delAAA=0, delAA=0, delA=0, dupA=0, dupAA=0

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 12	NC_000012.12:g.120763882_120763884del
GRCh38.p14 chr 12	NC_000012.12:g.120763883_120763884del
GRCh38.p14 chr 12	NC_000012.12:g.120763884del
GRCh38.p14 chr 12	NC_000012.12:g.120763884dup
GRCh38.p14 chr 12	NC_000012.12:g.120763883_120763884dup
GRCh37.p13 chr 12	NC_000012.11:g.121201685_121201687del
GRCh37.p13 chr 12	NC_000012.11:g.121201686_121201687del
GRCh37.p13 chr 12	NC_000012.11:g.121201687del
GRCh37.p13 chr 12	NC_000012.11:g.121201687dup
GRCh37.p13 chr 12	NC_000012.11:g.121201686_121201687dup

Gene: SPPL3, signal peptide peptidase like 3 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SPPL3 transcript	NM_139015.5:c.1115_1125=	N/A	3 Prime UTR Variant
SPPL3 transcript variant X1	XM_011537925.3:c.1115_1… XM_011537925.3:c.1115_1125=	N/A	3 Prime UTR Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(A)₁₁=	delAAA	delAA	delA	dupA	dupAA
GRCh38.p14 chr 12	NC_000012.12:g.120763874_120763884=	NC_000012.12:g.120763882_120763884del	NC_000012.12:g.120763883_120763884del	NC_000012.12:g.120763884del	NC_000012.12:g.120763884dup	NC_000012.12:g.120763883_120763884dup
GRCh37.p13 chr 12	NC_000012.11:g.121201677_121201687=	NC_000012.11:g.121201685_121201687del	NC_000012.11:g.121201686_121201687del	NC_000012.11:g.121201687del	NC_000012.11:g.121201687dup	NC_000012.11:g.121201686_121201687dup
SPPL3 transcript	NM_139015.5:c.1115_1125=	NM_139015.5:c.1123_1125del	NM_139015.5:c.1124_1125del	NM_139015.5:c.*1125del	NM_139015.5:c.*1125dup	NM_139015.5:c.1124_1125dup
SPPL3 transcript	NM_139015.4:c.1115_1125=	NM_139015.4:c.1123_1125del	NM_139015.4:c.1124_1125del	NM_139015.4:c.*1125del	NM_139015.4:c.*1125dup	NM_139015.4:c.1124_1125dup
SPPL3 transcript variant X1	XM_011537925.3:c.1115_1125=	XM_011537925.3:c.1123_1125del	XM_011537925.3:c.1124_1125del	XM_011537925.3:c.*1125del	XM_011537925.3:c.*1125dup	XM_011537925.3:c.1124_1125dup
SPPL3 transcript variant X1	XM_011537925.2:c.1115_1125=	XM_011537925.2:c.1123_1125del	XM_011537925.2:c.1124_1125del	XM_011537925.2:c.*1125del	XM_011537925.2:c.*1125dup	XM_011537925.2:c.1124_1125dup
SPPL3 transcript variant X2	XM_011537925.1:c.1115_1125=	XM_011537925.1:c.1123_1125del	XM_011537925.1:c.1124_1125del	XM_011537925.1:c.*1125del	XM_011537925.1:c.*1125dup	XM_011537925.1:c.1124_1125dup

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

75 SubSNP, 21 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss4309465	Jan 05, 2002 (102)
2	DEVINE_LAB	ss8061439	Mar 15, 2016 (147)
3	ABI	ss40109879	Mar 14, 2006 (137)
4	ABI	ss40258750	Mar 14, 2006 (126)
5	HGSV	ss81759598	Sep 08, 2015 (146)
6	HGSV	ss82699322	Sep 08, 2015 (146)
7	HGSV	ss83792689	Sep 08, 2015 (146)
8	DEVINE_LAB	ss94303445	Mar 15, 2016 (147)
9	BCMHGSC_JDW	ss103540418	Dec 06, 2013 (138)
10	BGI	ss104692606	Mar 15, 2016 (147)
11	BGI	ss105465460	Mar 15, 2016 (147)
12	GMI	ss155503310	Mar 15, 2016 (147)
13	BUSHMAN	ss193301671	Mar 15, 2016 (147)
14	GMI	ss287898896	Mar 15, 2016 (147)
15	GMI	ss289156278	May 04, 2012 (137)
16	GMI	ss289156279	May 04, 2012 (137)
17	PJP	ss294778212	Aug 21, 2014 (142)
18	PJP	ss294778213	May 09, 2011 (135)
19	PJP	ss294778214	May 09, 2011 (134)
20	BILGI_BIOE	ss666585906	Apr 25, 2013 (138)
21	1000GENOMES	ss1372710149	Aug 21, 2014 (142)
22	1000GENOMES	ss1372710150	Aug 21, 2014 (142)
23	1000GENOMES	ss1372710151	Aug 21, 2014 (142)
24	DDI	ss1536745271	Apr 01, 2015 (144)
25	EVA_UK10K_ALSPAC	ss1707651962	Apr 01, 2015 (144)
26	EVA_UK10K_TWINSUK	ss1707652343	Apr 01, 2015 (144)
27	EVA_UK10K_TWINSUK	ss1710583958	Apr 01, 2015 (144)
28	EVA_UK10K_ALSPAC	ss1710583986	Apr 01, 2015 (144)
29	HAMMER_LAB	ss1807450921	Sep 08, 2015 (146)
30	HAMMER_LAB	ss1807450922	Sep 08, 2015 (146)
31	TMC_SNPDB	ss1997056925	Jul 19, 2016 (147)
32	TMC_SNPDB	ss1997056927	Jul 19, 2016 (147)
33	SWEGEN	ss3010461868	Nov 08, 2017 (151)
34	BIOINF_KMB_FNS_UNIBA	ss3645280193	Oct 12, 2018 (152)
35	BIOINF_KMB_FNS_UNIBA	ss3645280194	Oct 12, 2018 (152)
36	BIOINF_KMB_FNS_UNIBA	ss3645280195	Oct 12, 2018 (152)
37	URBANLAB	ss3649935528	Oct 12, 2018 (152)
38	EVA_DECODE	ss3694607950	Jul 13, 2019 (153)
39	EVA_DECODE	ss3694607951	Jul 13, 2019 (153)
40	EVA_DECODE	ss3694607952	Jul 13, 2019 (153)
41	ACPOP	ss3739443229	Jul 13, 2019 (153)
42	ACPOP	ss3739443230	Jul 13, 2019 (153)
43	ACPOP	ss3739443231	Jul 13, 2019 (153)
44	PACBIO	ss3787354934	Jul 13, 2019 (153)
45	PACBIO	ss3792433842	Jul 13, 2019 (153)
46	PACBIO	ss3797316997	Jul 13, 2019 (153)
47	KHV_HUMAN_GENOMES	ss3816379277	Jul 13, 2019 (153)
48	KHV_HUMAN_GENOMES	ss3816379278	Jul 13, 2019 (153)
49	KHV_HUMAN_GENOMES	ss3816379279	Jul 13, 2019 (153)
50	EVA	ss3845740865	Apr 27, 2020 (154)
51	KOGIC	ss3972879831	Apr 27, 2020 (154)
52	KOGIC	ss3972879832	Apr 27, 2020 (154)
53	FSA-LAB	ss3984039257	Apr 26, 2021 (155)
54	EVA	ss3986061270	Apr 26, 2021 (155)
55	GNOMAD	ss4260221345	Apr 26, 2021 (155)
56	GNOMAD	ss4260221346	Apr 26, 2021 (155)
57	GNOMAD	ss4260221347	Apr 26, 2021 (155)
58	GNOMAD	ss4260221348	Apr 26, 2021 (155)
59	GNOMAD	ss4260221349	Apr 26, 2021 (155)
60	TOMMO_GENOMICS	ss5208487734	Apr 26, 2021 (155)
61	TOMMO_GENOMICS	ss5208487735	Apr 26, 2021 (155)
62	TOMMO_GENOMICS	ss5208487736	Apr 26, 2021 (155)
63	1000G_HIGH_COVERAGE	ss5292478868	Oct 16, 2022 (156)
64	1000G_HIGH_COVERAGE	ss5292478869	Oct 16, 2022 (156)
65	1000G_HIGH_COVERAGE	ss5292478870	Oct 16, 2022 (156)
66	1000G_HIGH_COVERAGE	ss5292478871	Oct 16, 2022 (156)
67	HUGCELL_USP	ss5487059280	Oct 16, 2022 (156)
68	HUGCELL_USP	ss5487059281	Oct 16, 2022 (156)
69	HUGCELL_USP	ss5487059282	Oct 16, 2022 (156)
70	TOMMO_GENOMICS	ss5758909523	Oct 16, 2022 (156)
71	TOMMO_GENOMICS	ss5758909524	Oct 16, 2022 (156)
72	TOMMO_GENOMICS	ss5758909525	Oct 16, 2022 (156)
73	EVA	ss5838609249	Oct 16, 2022 (156)
74	EVA	ss5838609250	Oct 16, 2022 (156)
75	EVA	ss5838609251	Oct 16, 2022 (156)
76	1000Genomes	NC_000012.11 - 121201677	Oct 12, 2018 (152)
77	The Avon Longitudinal Study of Parents and Children	NC_000012.11 - 121201677	Oct 12, 2018 (152)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 421343795 (NC_000012.12:120763873::A 3186/129732) Row 421343796 (NC_000012.12:120763873::AA 7/129796) Row 421343797 (NC_000012.12:120763873:A: 25328/129606)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 421343795 (NC_000012.12:120763873::A 3186/129732) Row 421343796 (NC_000012.12:120763873::AA 7/129796) Row 421343797 (NC_000012.12:120763873:A: 25328/129606)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 421343795 (NC_000012.12:120763873::A 3186/129732) Row 421343796 (NC_000012.12:120763873::AA 7/129796) Row 421343797 (NC_000012.12:120763873:A: 25328/129606)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 421343795 (NC_000012.12:120763873::A 3186/129732) Row 421343796 (NC_000012.12:120763873::AA 7/129796) Row 421343797 (NC_000012.12:120763873:A: 25328/129606)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 421343795 (NC_000012.12:120763873::A 3186/129732) Row 421343796 (NC_000012.12:120763873::AA 7/129796) Row 421343797 (NC_000012.12:120763873:A: 25328/129606)...	-	Apr 26, 2021 (155)
83	Korean Genome Project Submission ignored due to conflicting rows: Row 29257832 (NC_000012.12:120763873:AA: 1012/1832) Row 29257833 (NC_000012.12:120763874:A: 561/1832)	-	Apr 27, 2020 (154)
84	Korean Genome Project Submission ignored due to conflicting rows: Row 29257832 (NC_000012.12:120763873:AA: 1012/1832) Row 29257833 (NC_000012.12:120763874:A: 561/1832)	-	Apr 27, 2020 (154)
85	Northern Sweden Submission ignored due to conflicting rows: Row 12728094 (NC_000012.11:121201676:AA: 288/560) Row 12728095 (NC_000012.11:121201676:A: 44/560) Row 12728096 (NC_000012.11:121201676::A 10/560)	-	Jul 13, 2019 (153)
86	Northern Sweden Submission ignored due to conflicting rows: Row 12728094 (NC_000012.11:121201676:AA: 288/560) Row 12728095 (NC_000012.11:121201676:A: 44/560) Row 12728096 (NC_000012.11:121201676::A 10/560)	-	Jul 13, 2019 (153)
87	Northern Sweden Submission ignored due to conflicting rows: Row 12728094 (NC_000012.11:121201676:AA: 288/560) Row 12728095 (NC_000012.11:121201676:A: 44/560) Row 12728096 (NC_000012.11:121201676::A 10/560)	-	Jul 13, 2019 (153)
88	8.3KJPN Submission ignored due to conflicting rows: Row 66457041 (NC_000012.11:121201676:AA: 8592/16760) Row 66457042 (NC_000012.11:121201676:A: 4693/16760) Row 66457043 (NC_000012.11:121201676::A 27/16760)	-	Apr 26, 2021 (155)
89	8.3KJPN Submission ignored due to conflicting rows: Row 66457041 (NC_000012.11:121201676:AA: 8592/16760) Row 66457042 (NC_000012.11:121201676:A: 4693/16760) Row 66457043 (NC_000012.11:121201676::A 27/16760)	-	Apr 26, 2021 (155)
90	8.3KJPN Submission ignored due to conflicting rows: Row 66457041 (NC_000012.11:121201676:AA: 8592/16760) Row 66457042 (NC_000012.11:121201676:A: 4693/16760) Row 66457043 (NC_000012.11:121201676::A 27/16760)	-	Apr 26, 2021 (155)
91	14KJPN Submission ignored due to conflicting rows: Row 92746627 (NC_000012.12:120763873:AA: 14519/28258) Row 92746628 (NC_000012.12:120763873:A: 7932/28258) Row 92746629 (NC_000012.12:120763873::A 42/28258)	-	Oct 16, 2022 (156)
92	14KJPN Submission ignored due to conflicting rows: Row 92746627 (NC_000012.12:120763873:AA: 14519/28258) Row 92746628 (NC_000012.12:120763873:A: 7932/28258) Row 92746629 (NC_000012.12:120763873::A 42/28258)	-	Oct 16, 2022 (156)
93	14KJPN Submission ignored due to conflicting rows: Row 92746627 (NC_000012.12:120763873:AA: 14519/28258) Row 92746628 (NC_000012.12:120763873:A: 7932/28258) Row 92746629 (NC_000012.12:120763873::A 42/28258)	-	Oct 16, 2022 (156)
94	UK 10K study - Twins	-	Oct 12, 2018 (152)
95	UK 10K study - Twins Submission ignored due to conflicting rows: Row 33180902 (NC_000012.11:121201676:AA: 1933/3708) Row 33180903 (NC_000012.11:121201677:A: 315/3708)	-	Apr 27, 2020 (154)
96	ALFA	NC_000012.12 - 120763874	Apr 26, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID	History Updated (Build)
rs148545785	Sep 17, 2011 (135)
rs199631960	May 11, 2012 (137)
rs77605918	Oct 17, 2011 (136)
rs34734203	May 04, 2012 (137)
rs35071578	May 23, 2006 (127)
rs66535729	Jul 30, 2012 (137)
rs112933056	Oct 12, 2011 (135)
rs201513670	May 11, 2012 (137)
rs33966367	May 23, 2006 (127)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss3984039257	NC_000012.11:121201676:AAA:	NC_000012.12:120763873:AAAAAAAAAAA… NC_000012.12:120763873:AAAAAAAAAAA:AAAAAAAA	(self)
ss4260221349, ss5292478871	NC_000012.12:120763873:AAA:	NC_000012.12:120763873:AAAAAAAAAAA… NC_000012.12:120763873:AAAAAAAAAAA:AAAAAAAA	(self)
2676191121	NC_000012.12:120763873:AAAAAAAAAAA… NC_000012.12:120763873:AAAAAAAAAAA:AAAAAAAA	NC_000012.12:120763873:AAAAAAAAAAA… NC_000012.12:120763873:AAAAAAAAAAA:AAAAAAAA	(self)
ss4309465	NT_009775.17:11778214:AAA:	NC_000012.12:120763873:AAAAAAAAAAA… NC_000012.12:120763873:AAAAAAAAAAA:AAAAAAAA	(self)
ss81759598, ss82699322, ss83792689	NC_000012.9:119664405:AA:	NC_000012.12:120763873:AAAAAAAAAAA… NC_000012.12:120763873:AAAAAAAAAAA:AAAAAAAAA	(self)
ss289156279, ss294778212	NC_000012.10:119686059:AA:	NC_000012.12:120763873:AAAAAAAAAAA… NC_000012.12:120763873:AAAAAAAAAAA:AAAAAAAAA	(self)
ss294778213	NC_000012.10:119686068:AA:	NC_000012.12:120763873:AAAAAAAAAAA… NC_000012.12:120763873:AAAAAAAAAAA:AAAAAAAAA	(self)
59735035, 33180902, ss666585906, ss1372710149, ss1536745271, ss1707651962, ss1707652343, ss1807450922, ss3010461868, ss3739443229, ss3787354934, ss3792433842, ss3797316997, ss5208487734, ss5838609249	NC_000012.11:121201676:AA:	NC_000012.12:120763873:AAAAAAAAAAA… NC_000012.12:120763873:AAAAAAAAAAA:AAAAAAAAA	(self)
ss3645280193, ss3649935528, ss3694607952, ss3816379277, ss3972879831, ss4260221348, ss5292478870, ss5487059281, ss5758909523	NC_000012.12:120763873:AA:	NC_000012.12:120763873:AAAAAAAAAAA… NC_000012.12:120763873:AAAAAAAAAAA:AAAAAAAAA	(self)
2676191121	NC_000012.12:120763873:AAAAAAAAAAA… NC_000012.12:120763873:AAAAAAAAAAA:AAAAAAAAA	NC_000012.12:120763873:AAAAAAAAAAA… NC_000012.12:120763873:AAAAAAAAAAA:AAAAAAAAA	(self)
ss8061439, ss193301671, ss287898896	NT_009775.17:11778206:AA:	NC_000012.12:120763873:AAAAAAAAAAA… NC_000012.12:120763873:AAAAAAAAAAA:AAAAAAAAA	(self)
ss104692606, ss105465460	NT_009775.17:11778214:AA:	NC_000012.12:120763873:AAAAAAAAAAA… NC_000012.12:120763873:AAAAAAAAAAA:AAAAAAAAA	(self)
ss94303445, ss103540418, ss155503310	NT_009775.17:11778215:AA:	NC_000012.12:120763873:AAAAAAAAAAA… NC_000012.12:120763873:AAAAAAAAAAA:AAAAAAAAA	(self)
ss289156278	NC_000012.10:119686059:A:	NC_000012.12:120763873:AAAAAAAAAAA… NC_000012.12:120763873:AAAAAAAAAAA:AAAAAAAAAA	(self)
ss294778214	NC_000012.10:119686069:A:	NC_000012.12:120763873:AAAAAAAAAAA… NC_000012.12:120763873:AAAAAAAAAAA:AAAAAAAAAA	(self)
ss1807450921, ss3739443230, ss3986061270, ss5208487735, ss5838609251	NC_000012.11:121201676:A:	NC_000012.12:120763873:AAAAAAAAAAA… NC_000012.12:120763873:AAAAAAAAAAA:AAAAAAAAAA	(self)
ss1372710150, ss1710583958, ss1710583986, ss1997056927	NC_000012.11:121201677:A:	NC_000012.12:120763873:AAAAAAAAAAA… NC_000012.12:120763873:AAAAAAAAAAA:AAAAAAAAAA	(self)
ss3645280194, ss3845740865, ss4260221347, ss5292478868, ss5487059280, ss5758909524	NC_000012.12:120763873:A:	NC_000012.12:120763873:AAAAAAAAAAA… NC_000012.12:120763873:AAAAAAAAAAA:AAAAAAAAAA	(self)
2676191121	NC_000012.12:120763873:AAAAAAAAAAA… NC_000012.12:120763873:AAAAAAAAAAA:AAAAAAAAAA	NC_000012.12:120763873:AAAAAAAAAAA… NC_000012.12:120763873:AAAAAAAAAAA:AAAAAAAAAA	(self)
ss3694607951, ss3816379279, ss3972879832	NC_000012.12:120763874:A:	NC_000012.12:120763873:AAAAAAAAAAA… NC_000012.12:120763873:AAAAAAAAAAA:AAAAAAAAAA	(self)
ss40109879, ss40258750	NT_009775.17:11778206:A:	NC_000012.12:120763873:AAAAAAAAAAA… NC_000012.12:120763873:AAAAAAAAAAA:AAAAAAAAAA	(self)
ss3739443231, ss5208487736, ss5838609250	NC_000012.11:121201676::A	NC_000012.12:120763873:AAAAAAAAAAA… NC_000012.12:120763873:AAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss1372710151, ss1997056925	NC_000012.11:121201678::A	NC_000012.12:120763873:AAAAAAAAAAA… NC_000012.12:120763873:AAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3645280195, ss4260221345, ss5292478869, ss5487059282, ss5758909525	NC_000012.12:120763873::A	NC_000012.12:120763873:AAAAAAAAAAA… NC_000012.12:120763873:AAAAAAAAAAA:AAAAAAAAAAAA	(self)
2676191121	NC_000012.12:120763873:AAAAAAAAAAA… NC_000012.12:120763873:AAAAAAAAAAA:AAAAAAAAAAAA	NC_000012.12:120763873:AAAAAAAAAAA… NC_000012.12:120763873:AAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3694607950, ss3816379278	NC_000012.12:120763875::A	NC_000012.12:120763873:AAAAAAAAAAA… NC_000012.12:120763873:AAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4260221346	NC_000012.12:120763873::AA	NC_000012.12:120763873:AAAAAAAAAAA… NC_000012.12:120763873:AAAAAAAAAAA:AAAAAAAAAAAAA	(self)
2676191121	NC_000012.12:120763873:AAAAAAAAAAA… NC_000012.12:120763873:AAAAAAAAAAA:AAAAAAAAAAAAA	NC_000012.12:120763873:AAAAAAAAAAA… NC_000012.12:120763873:AAAAAAAAAAA:AAAAAAAAAAAAA	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs3078036

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
Top▲ Help
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs3078036