Name: rs61618174
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.

rs61618174

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:37680997-37681008 (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: delCC / delC / dupC / dupCC / dupC…
delCC / delC / dupC / dupCC / dupCCC
Variation Type: Indel Insertion and Deletion
Frequency: delC=0.2185 (1716/7854, ALFA)
delC=0.4411 (2209/5008, 1000G)
(C)₁₂=0.47 (19/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: MDGA1 : Intron 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	7854	CCCCCCCCCCCC=0.7502	CCCCCCCCCC=0.0000, CCCCCCCCCCC=0.2185, CCCCCCCCCCCCC=0.0307, CCCCCCCCCCCCCC=0.0006, CCCCCCCCCCCCCCC=0.0000	0.652951	0.09177	0.255279	32
European	Sub	6782	CCCCCCCCCCCC=0.7114	CCCCCCCCCC=0.0000, CCCCCCCCCCC=0.2524, CCCCCCCCCCCCC=0.0355, CCCCCCCCCCCCCC=0.0006, CCCCCCCCCCCCCCC=0.0000	0.594808	0.106996	0.298196	32
African	Sub	626	CCCCCCCCCCCC=1.000	CCCCCCCCCC=0.000, CCCCCCCCCCC=0.000, CCCCCCCCCCCCC=0.000, CCCCCCCCCCCCCC=0.000, CCCCCCCCCCCCCCC=0.000	1.0	0.0	0.0	N/A
African Others	Sub	22	CCCCCCCCCCCC=1.00	CCCCCCCCCC=0.00, CCCCCCCCCCC=0.00, CCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCCC=0.00	1.0	0.0	0.0	N/A
African American	Sub	604	CCCCCCCCCCCC=1.000	CCCCCCCCCC=0.000, CCCCCCCCCCC=0.000, CCCCCCCCCCCCC=0.000, CCCCCCCCCCCCCC=0.000, CCCCCCCCCCCCCCC=0.000	1.0	0.0	0.0	N/A
Asian	Sub	16	CCCCCCCCCCCC=1.00	CCCCCCCCCC=0.00, CCCCCCCCCCC=0.00, CCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCCC=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	8	CCCCCCCCCCCC=1.0	CCCCCCCCCC=0.0, CCCCCCCCCCC=0.0, CCCCCCCCCCCCC=0.0, CCCCCCCCCCCCCC=0.0, CCCCCCCCCCCCCCC=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	8	CCCCCCCCCCCC=1.0	CCCCCCCCCC=0.0, CCCCCCCCCCC=0.0, CCCCCCCCCCCCC=0.0, CCCCCCCCCCCCCC=0.0, CCCCCCCCCCCCCCC=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	44	CCCCCCCCCCCC=1.00	CCCCCCCCCC=0.00, CCCCCCCCCCC=0.00, CCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCCC=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	204	CCCCCCCCCCCC=1.000	CCCCCCCCCC=0.000, CCCCCCCCCCC=0.000, CCCCCCCCCCCCC=0.000, CCCCCCCCCCCCCC=0.000, CCCCCCCCCCCCCCC=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	26	CCCCCCCCCCCC=1.00	CCCCCCCCCC=0.00, CCCCCCCCCCC=0.00, CCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCC=0.00, CCCCCCCCCCCCCCC=0.00	1.0	0.0	0.0	N/A
Other	Sub	156	CCCCCCCCCCCC=0.968	CCCCCCCCCC=0.000, CCCCCCCCCCC=0.026, CCCCCCCCCCCCC=0.000, CCCCCCCCCCCCCC=0.006, CCCCCCCCCCCCCCC=0.000	0.974026	0.012987	0.012987	18

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
Allele Frequency Aggregator	Total	Global	7854	(C)₁₂=0.7502	delCC=0.0000, delC=0.2185, dupC=0.0307, dupCC=0.0006, dupCCC=0.0000
Allele Frequency Aggregator	European	Sub	6782	(C)₁₂=0.7114	delCC=0.0000, delC=0.2524, dupC=0.0355, dupCC=0.0006, dupCCC=0.0000
Allele Frequency Aggregator	African	Sub	626	(C)₁₂=1.000	delCC=0.000, delC=0.000, dupC=0.000, dupCC=0.000, dupCCC=0.000
Allele Frequency Aggregator	Latin American 2	Sub	204	(C)₁₂=1.000	delCC=0.000, delC=0.000, dupC=0.000, dupCC=0.000, dupCCC=0.000
Allele Frequency Aggregator	Other	Sub	156	(C)₁₂=0.968	delCC=0.000, delC=0.026, dupC=0.000, dupCC=0.006, dupCCC=0.000
Allele Frequency Aggregator	Latin American 1	Sub	44	(C)₁₂=1.00	delCC=0.00, delC=0.00, dupC=0.00, dupCC=0.00, dupCCC=0.00
Allele Frequency Aggregator	South Asian	Sub	26	(C)₁₂=1.00	delCC=0.00, delC=0.00, dupC=0.00, dupCC=0.00, dupCCC=0.00
Allele Frequency Aggregator	Asian	Sub	16	(C)₁₂=1.00	delCC=0.00, delC=0.00, dupC=0.00, dupCC=0.00, dupCCC=0.00
1000Genomes	Global	Study-wide	5008	(C)₁₂=0.5589	delC=0.4411
1000Genomes	African	Sub	1322	(C)₁₂=0.5998	delC=0.4002
1000Genomes	East Asian	Sub	1008	(C)₁₂=0.4018	delC=0.5982
1000Genomes	Europe	Sub	1006	(C)₁₂=0.5984	delC=0.4016
1000Genomes	South Asian	Sub	978	(C)₁₂=0.594	delC=0.406
1000Genomes	American	Sub	694	(C)₁₂=0.602	delC=0.398
The Danish reference pan genome	Danish	Study-wide	40	(C)₁₂=0.47	delC=0.53

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 6	NC_000006.12:g.37681007_37681008del
GRCh38.p14 chr 6	NC_000006.12:g.37681008del
GRCh38.p14 chr 6	NC_000006.12:g.37681008dup
GRCh38.p14 chr 6	NC_000006.12:g.37681007_37681008dup
GRCh38.p14 chr 6	NC_000006.12:g.37681006_37681008dup
GRCh37.p13 chr 6	NC_000006.11:g.37648783_37648784del
GRCh37.p13 chr 6	NC_000006.11:g.37648784del
GRCh37.p13 chr 6	NC_000006.11:g.37648784dup
GRCh37.p13 chr 6	NC_000006.11:g.37648783_37648784dup
GRCh37.p13 chr 6	NC_000006.11:g.37648782_37648784dup
MDGA1 RefSeqGene	NG_051764.1:g.21993_21994del
MDGA1 RefSeqGene	NG_051764.1:g.21994del
MDGA1 RefSeqGene	NG_051764.1:g.21994dup
MDGA1 RefSeqGene	NG_051764.1:g.21993_21994dup
MDGA1 RefSeqGene	NG_051764.1:g.21992_21994dup

Gene: MDGA1, MAM domain containing glycosylphosphatidylinositol anchor 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
MDGA1 transcript	NM_153487.4:c.67+15747_67… NM_153487.4:c.67+15747_67+15748del	N/A	Intron Variant
MDGA1 transcript variant X1	XM_006715056.4:c.67+15747… XM_006715056.4:c.67+15747_67+15748del	N/A	Intron Variant
MDGA1 transcript variant X2	XM_017010734.2:c.67+15747… XM_017010734.2:c.67+15747_67+15748del	N/A	Intron Variant
MDGA1 transcript variant X3	XM_047418637.1:c.-102+133… XM_047418637.1:c.-102+13392_-102+13393del	N/A	Intron Variant
MDGA1 transcript variant X5	XM_047418638.1:c.67+15747… XM_047418638.1:c.67+15747_67+15748del	N/A	Intron Variant
MDGA1 transcript variant X4	XR_926141.3:n.	N/A	Intron 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	(C)₁₂=	delCC	delC	dupC	dupCC	dupCCC
GRCh38.p14 chr 6	NC_000006.12:g.37680997_37681008=	NC_000006.12:g.37681007_37681008del	NC_000006.12:g.37681008del	NC_000006.12:g.37681008dup	NC_000006.12:g.37681007_37681008dup	NC_000006.12:g.37681006_37681008dup
GRCh37.p13 chr 6	NC_000006.11:g.37648773_37648784=	NC_000006.11:g.37648783_37648784del	NC_000006.11:g.37648784del	NC_000006.11:g.37648784dup	NC_000006.11:g.37648783_37648784dup	NC_000006.11:g.37648782_37648784dup
MDGA1 RefSeqGene	NG_051764.1:g.21983_21994=	NG_051764.1:g.21993_21994del	NG_051764.1:g.21994del	NG_051764.1:g.21994dup	NG_051764.1:g.21993_21994dup	NG_051764.1:g.21992_21994dup
MDGA1 transcript	NM_153487.3:c.67+15748=	NM_153487.3:c.67+15747_67+15748del	NM_153487.3:c.67+15748del	NM_153487.3:c.67+15748dup	NM_153487.3:c.67+15747_67+15748dup	NM_153487.3:c.67+15746_67+15748dup
MDGA1 transcript	NM_153487.4:c.67+15748=	NM_153487.4:c.67+15747_67+15748del	NM_153487.4:c.67+15748del	NM_153487.4:c.67+15748dup	NM_153487.4:c.67+15747_67+15748dup	NM_153487.4:c.67+15746_67+15748dup
MDGA1 transcript variant X1	XM_005249003.1:c.67+15748=	XM_005249003.1:c.67+15747_67+15748del	XM_005249003.1:c.67+15748del	XM_005249003.1:c.67+15748dup	XM_005249003.1:c.67+15747_67+15748dup	XM_005249003.1:c.67+15746_67+15748dup
MDGA1 transcript variant X1	XM_006715056.4:c.67+15748=	XM_006715056.4:c.67+15747_67+15748del	XM_006715056.4:c.67+15748del	XM_006715056.4:c.67+15748dup	XM_006715056.4:c.67+15747_67+15748dup	XM_006715056.4:c.67+15746_67+15748dup
MDGA1 transcript variant X2	XM_017010734.2:c.67+15748=	XM_017010734.2:c.67+15747_67+15748del	XM_017010734.2:c.67+15748del	XM_017010734.2:c.67+15748dup	XM_017010734.2:c.67+15747_67+15748dup	XM_017010734.2:c.67+15746_67+15748dup
MDGA1 transcript variant X3	XM_047418637.1:c.-102+13393=	XM_047418637.1:c.-102+13392_-102+13393del	XM_047418637.1:c.-102+13393del	XM_047418637.1:c.-102+13393dup	XM_047418637.1:c.-102+13392_-102+13393dup	XM_047418637.1:c.-102+13391_-102+13393dup
MDGA1 transcript variant X5	XM_047418638.1:c.67+15748=	XM_047418638.1:c.67+15747_67+15748del	XM_047418638.1:c.67+15748del	XM_047418638.1:c.67+15748dup	XM_047418638.1:c.67+15747_67+15748dup	XM_047418638.1:c.67+15746_67+15748dup

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#.

47 SubSNP, 21 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss82064379	Dec 16, 2007 (129)
2	HGSV	ss82142210	Dec 16, 2007 (129)
3	HUMANGENOME_JCVI	ss95426013	Oct 12, 2018 (152)
4	PJP	ss295275843	Oct 12, 2018 (152)
5	SSMP	ss663693489	Apr 01, 2015 (144)
6	1000GENOMES	ss1375391116	Aug 21, 2014 (142)
7	EVA_GENOME_DK	ss1576730905	Apr 01, 2015 (144)
8	HAMMER_LAB	ss1804386685	Sep 08, 2015 (146)
9	SWEGEN	ss2998909733	Nov 08, 2017 (151)
10	BEROUKHIMLAB	ss3644209482	Oct 12, 2018 (152)
11	BEROUKHIMLAB	ss3644209483	Oct 12, 2018 (152)
12	BIOINF_KMB_FNS_UNIBA	ss3645948905	Oct 12, 2018 (152)
13	URBANLAB	ss3648330955	Oct 12, 2018 (152)
14	EVA_DECODE	ss3717020215	Jul 13, 2019 (153)
15	EVA_DECODE	ss3717020216	Jul 13, 2019 (153)
16	EVA_DECODE	ss3717020217	Jul 13, 2019 (153)
17	ACPOP	ss3733419471	Jul 13, 2019 (153)
18	ACPOP	ss3733419472	Jul 13, 2019 (153)
19	ACPOP	ss3733419473	Jul 13, 2019 (153)
20	PACBIO	ss3785448466	Jul 13, 2019 (153)
21	PACBIO	ss3790803597	Jul 13, 2019 (153)
22	PACBIO	ss3795682220	Jul 13, 2019 (153)
23	KHV_HUMAN_GENOMES	ss3808052179	Jul 13, 2019 (153)
24	EVA	ss3829873903	Apr 26, 2020 (154)
25	KOGIC	ss3958834181	Apr 26, 2020 (154)
26	KOGIC	ss3958834182	Apr 26, 2020 (154)
27	KOGIC	ss3958834183	Apr 26, 2020 (154)
28	GNOMAD	ss4140088072	Apr 26, 2021 (155)
29	GNOMAD	ss4140088073	Apr 26, 2021 (155)
30	GNOMAD	ss4140088074	Apr 26, 2021 (155)
31	GNOMAD	ss4140088075	Apr 26, 2021 (155)
32	GNOMAD	ss4140088076	Apr 26, 2021 (155)
33	TOMMO_GENOMICS	ss5177075230	Apr 26, 2021 (155)
34	TOMMO_GENOMICS	ss5177075231	Apr 26, 2021 (155)
35	TOMMO_GENOMICS	ss5177075232	Apr 26, 2021 (155)
36	1000G_HIGH_COVERAGE	ss5268107582	Oct 13, 2022 (156)
37	HUGCELL_USP	ss5465812794	Oct 13, 2022 (156)
38	HUGCELL_USP	ss5465812795	Oct 13, 2022 (156)
39	HUGCELL_USP	ss5465812796	Oct 13, 2022 (156)
40	HUGCELL_USP	ss5465812797	Oct 13, 2022 (156)
41	TOMMO_GENOMICS	ss5714996970	Oct 13, 2022 (156)
42	TOMMO_GENOMICS	ss5714996971	Oct 13, 2022 (156)
43	TOMMO_GENOMICS	ss5714996972	Oct 13, 2022 (156)
44	TOMMO_GENOMICS	ss5714996973	Oct 13, 2022 (156)
45	EVA	ss5842108426	Oct 13, 2022 (156)
46	EVA	ss5842108427	Oct 13, 2022 (156)
47	EVA	ss5855316926	Oct 13, 2022 (156)
48	1000Genomes	NC_000006.11 - 37648773	Oct 12, 2018 (152)
49	The Danish reference pan genome	NC_000006.11 - 37648773	Apr 26, 2020 (154)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222427892 (NC_000006.12:37680996::C 11000/133254) Row 222427893 (NC_000006.12:37680996::CC 598/133820) Row 222427894 (NC_000006.12:37680996::CCC 45/133936)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222427892 (NC_000006.12:37680996::C 11000/133254) Row 222427893 (NC_000006.12:37680996::CC 598/133820) Row 222427894 (NC_000006.12:37680996::CCC 45/133936)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222427892 (NC_000006.12:37680996::C 11000/133254) Row 222427893 (NC_000006.12:37680996::CC 598/133820) Row 222427894 (NC_000006.12:37680996::CCC 45/133936)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222427892 (NC_000006.12:37680996::C 11000/133254) Row 222427893 (NC_000006.12:37680996::CC 598/133820) Row 222427894 (NC_000006.12:37680996::CCC 45/133936)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 222427892 (NC_000006.12:37680996::C 11000/133254) Row 222427893 (NC_000006.12:37680996::CC 598/133820) Row 222427894 (NC_000006.12:37680996::CCC 45/133936)...	-	Apr 26, 2021 (155)
55	Korean Genome Project Submission ignored due to conflicting rows: Row 15212182 (NC_000006.12:37680996:C: 775/1814) Row 15212183 (NC_000006.12:37680997::C 413/1814) Row 15212184 (NC_000006.12:37680997::CC 16/1814)	-	Apr 26, 2020 (154)
56	Korean Genome Project Submission ignored due to conflicting rows: Row 15212182 (NC_000006.12:37680996:C: 775/1814) Row 15212183 (NC_000006.12:37680997::C 413/1814) Row 15212184 (NC_000006.12:37680997::CC 16/1814)	-	Apr 26, 2020 (154)
57	Korean Genome Project Submission ignored due to conflicting rows: Row 15212182 (NC_000006.12:37680996:C: 775/1814) Row 15212183 (NC_000006.12:37680997::C 413/1814) Row 15212184 (NC_000006.12:37680997::CC 16/1814)	-	Apr 26, 2020 (154)
58	Northern Sweden Submission ignored due to conflicting rows: Row 6704336 (NC_000006.11:37648772:C: 233/600) Row 6704337 (NC_000006.11:37648772::C 38/600) Row 6704338 (NC_000006.11:37648772::CC 6/600)	-	Jul 13, 2019 (153)
59	Northern Sweden Submission ignored due to conflicting rows: Row 6704336 (NC_000006.11:37648772:C: 233/600) Row 6704337 (NC_000006.11:37648772::C 38/600) Row 6704338 (NC_000006.11:37648772::CC 6/600)	-	Jul 13, 2019 (153)
60	Northern Sweden Submission ignored due to conflicting rows: Row 6704336 (NC_000006.11:37648772:C: 233/600) Row 6704337 (NC_000006.11:37648772::C 38/600) Row 6704338 (NC_000006.11:37648772::CC 6/600)	-	Jul 13, 2019 (153)
61	8.3KJPN Submission ignored due to conflicting rows: Row 35044537 (NC_000006.11:37648772:C: 6507/16632) Row 35044538 (NC_000006.11:37648772::C 3157/16632) Row 35044539 (NC_000006.11:37648772::CC 50/16632)	-	Apr 26, 2021 (155)
62	8.3KJPN Submission ignored due to conflicting rows: Row 35044537 (NC_000006.11:37648772:C: 6507/16632) Row 35044538 (NC_000006.11:37648772::C 3157/16632) Row 35044539 (NC_000006.11:37648772::CC 50/16632)	-	Apr 26, 2021 (155)
63	8.3KJPN Submission ignored due to conflicting rows: Row 35044537 (NC_000006.11:37648772:C: 6507/16632) Row 35044538 (NC_000006.11:37648772::C 3157/16632) Row 35044539 (NC_000006.11:37648772::CC 50/16632)	-	Apr 26, 2021 (155)
64	14KJPN Submission ignored due to conflicting rows: Row 48834074 (NC_000006.12:37680996::C 5814/28232) Row 48834075 (NC_000006.12:37680996:C: 10920/28232) Row 48834076 (NC_000006.12:37680996::CC 81/28232)...	-	Oct 13, 2022 (156)
65	14KJPN Submission ignored due to conflicting rows: Row 48834074 (NC_000006.12:37680996::C 5814/28232) Row 48834075 (NC_000006.12:37680996:C: 10920/28232) Row 48834076 (NC_000006.12:37680996::CC 81/28232)...	-	Oct 13, 2022 (156)
66	14KJPN Submission ignored due to conflicting rows: Row 48834074 (NC_000006.12:37680996::C 5814/28232) Row 48834075 (NC_000006.12:37680996:C: 10920/28232) Row 48834076 (NC_000006.12:37680996::CC 81/28232)...	-	Oct 13, 2022 (156)
67	14KJPN Submission ignored due to conflicting rows: Row 48834074 (NC_000006.12:37680996::C 5814/28232) Row 48834075 (NC_000006.12:37680996:C: 10920/28232) Row 48834076 (NC_000006.12:37680996::CC 81/28232)...	-	Oct 13, 2022 (156)
68	ALFA	NC_000006.12 - 37680997	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)
rs72431105	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss5842108427	NC_000006.11:37648772:CC:	NC_000006.12:37680996:CCCCCCCCCCCC… NC_000006.12:37680996:CCCCCCCCCCCC:CCCCCCCCCC
ss4140088076, ss5465812796, ss5714996973	NC_000006.12:37680996:CC:	NC_000006.12:37680996:CCCCCCCCCCCC… NC_000006.12:37680996:CCCCCCCCCCCC:CCCCCCCCCC	(self)
444334715	NC_000006.12:37680996:CCCCCCCCCCCC… NC_000006.12:37680996:CCCCCCCCCCCC:CCCCCCCCCC	NC_000006.12:37680996:CCCCCCCCCCCC… NC_000006.12:37680996:CCCCCCCCCCCC:CCCCCCCCCC	(self)
ss82064379, ss82142210	NC_000006.9:37756761:C:	NC_000006.12:37680996:CCCCCCCCCCCC… NC_000006.12:37680996:CCCCCCCCCCCC:CCCCCCCCCCC	(self)
31517903, 1069303, ss663693489, ss1375391116, ss1576730905, ss1804386685, ss2998909733, ss3644209482, ss3733419471, ss3785448466, ss3790803597, ss3795682220, ss3829873903, ss5177075230, ss5842108426	NC_000006.11:37648772:C:	NC_000006.12:37680996:CCCCCCCCCCCC… NC_000006.12:37680996:CCCCCCCCCCCC:CCCCCCCCCCC	(self)
ss3645948905, ss3648330955, ss3717020217, ss3808052179, ss3958834181, ss4140088075, ss5465812794, ss5714996971, ss5855316926	NC_000006.12:37680996:C:	NC_000006.12:37680996:CCCCCCCCCCCC… NC_000006.12:37680996:CCCCCCCCCCCC:CCCCCCCCCCC	(self)
444334715	NC_000006.12:37680996:CCCCCCCCCCCC… NC_000006.12:37680996:CCCCCCCCCCCC:CCCCCCCCCCC	NC_000006.12:37680996:CCCCCCCCCCCC… NC_000006.12:37680996:CCCCCCCCCCCC:CCCCCCCCCCC	(self)
ss295275843	NC_000006.10:37756756::C	NC_000006.12:37680996:CCCCCCCCCCCC… NC_000006.12:37680996:CCCCCCCCCCCC:CCCCCCCCCCCCC	(self)
ss3644209483, ss3733419472, ss5177075231	NC_000006.11:37648772::C	NC_000006.12:37680996:CCCCCCCCCCCC… NC_000006.12:37680996:CCCCCCCCCCCC:CCCCCCCCCCCCC	(self)
ss4140088072, ss5268107582, ss5465812795, ss5714996970	NC_000006.12:37680996::C	NC_000006.12:37680996:CCCCCCCCCCCC… NC_000006.12:37680996:CCCCCCCCCCCC:CCCCCCCCCCCCC	(self)
444334715	NC_000006.12:37680996:CCCCCCCCCCCC… NC_000006.12:37680996:CCCCCCCCCCCC:CCCCCCCCCCCCC	NC_000006.12:37680996:CCCCCCCCCCCC… NC_000006.12:37680996:CCCCCCCCCCCC:CCCCCCCCCCCCC	(self)
ss3717020216, ss3958834182	NC_000006.12:37680997::C	NC_000006.12:37680996:CCCCCCCCCCCC… NC_000006.12:37680996:CCCCCCCCCCCC:CCCCCCCCCCCCC	(self)
ss95426013	NT_007592.15:37588784::C	NC_000006.12:37680996:CCCCCCCCCCCC… NC_000006.12:37680996:CCCCCCCCCCCC:CCCCCCCCCCCCC	(self)
ss3733419473, ss5177075232	NC_000006.11:37648772::CC	NC_000006.12:37680996:CCCCCCCCCCCC… NC_000006.12:37680996:CCCCCCCCCCCC:CCCCCCCCCCCCCC	(self)
ss4140088073, ss5465812797, ss5714996972	NC_000006.12:37680996::CC	NC_000006.12:37680996:CCCCCCCCCCCC… NC_000006.12:37680996:CCCCCCCCCCCC:CCCCCCCCCCCCCC	(self)
444334715	NC_000006.12:37680996:CCCCCCCCCCCC… NC_000006.12:37680996:CCCCCCCCCCCC:CCCCCCCCCCCCCC	NC_000006.12:37680996:CCCCCCCCCCCC… NC_000006.12:37680996:CCCCCCCCCCCC:CCCCCCCCCCCCCC	(self)
ss3717020215, ss3958834183	NC_000006.12:37680997::CC	NC_000006.12:37680996:CCCCCCCCCCCC… NC_000006.12:37680996:CCCCCCCCCCCC:CCCCCCCCCCCCCC	(self)
ss4140088074	NC_000006.12:37680996::CCC	NC_000006.12:37680996:CCCCCCCCCCCC… NC_000006.12:37680996:CCCCCCCCCCCC:CCCCCCCCCCCCCCC	(self)
444334715	NC_000006.12:37680996:CCCCCCCCCCCC… NC_000006.12:37680996:CCCCCCCCCCCC:CCCCCCCCCCCCCCC	NC_000006.12:37680996:CCCCCCCCCCCC… NC_000006.12:37680996:CCCCCCCCCCCC:CCCCCCCCCCCCCCC	(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 rs61618174

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

rs61618174